A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516984



Internal ID15444277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:23100321..23106570hg38UCSC Ensembl
Innerchr7:23139940..23146189hg19UCSC Ensembl
Innerchr7:23106465..23112714hg18UCSC Ensembl
Innerchr7:22913180..22919429hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg386250
hg196250
hg186250
hg176250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685827, nssv664242, nssv683632, nssv687037, nssv667100, nssv665678, nssv652912, nssv670518, nssv652640, nssv656987, nssv688917, nssv653554, nssv662783, nssv671482, nssv668569, nssv688535, nssv652494, nssv679207, nssv653066, nssv659581, nssv672274, nssv660916, nssv655318, nssv677162, nssv674916, nssv683966, nssv689407, nssv686850, nssv663177, nssv656556, nssv675187, nssv652676, nssv677005, nssv690419, nssv675456, nssv692953, nssv681515, nssv659845, nssv659545, nssv658730, nssv669985, nssv680402, nssv688077, nssv660281, nssv697054, nssv668160, nssv683631, nssv665541, nssv688235, nssv677881, nssv691560, nssv690466, nssv664997, nssv665812
Samples
Known GenesKLHL7, KLHL7-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516984
Frequency
Sample Size2026
Observed Gain0
Observed Loss54
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer