A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683935



Internal ID15420587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62715937..62892897hg38UCSC Ensembl
Innerchr7:62176315..62353275hg19UCSC Ensembl
Innerchr7:61813750..61990710hg18UCSC Ensembl
Innerchr7:61620465..61797425hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38176961
hg19176961
hg18176961
hg17176961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683935
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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