A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608992



Internal ID16396401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150348821..150418095hg38UCSC Ensembl
Innerchr7:150045910..150115183hg19UCSC Ensembl
Innerchr7:149676843..149746116hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3869275
hg1969274
hg1869274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11718n54
Supporting Variantsnssv1099479
Samples
Known GenesLOC728743, REPIN1, RNU6-33P, RNU6-34P, ZNF775
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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