A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952215



Internal ID16954402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:156524609..156527308hg38UCSC Ensembl
Outerchr1:156494401..156497100hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998201
SamplesBILGI_BIOE
Known GenesIQGAP3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952215
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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