A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666769



Internal ID15403421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128843173..128911686hg38UCSC Ensembl
Innerchr7:128483227..128551740hg19UCSC Ensembl
Innerchr7:128270463..128338976hg18UCSC Ensembl
Innerchr7:128077178..128145691hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3868514
hg1968514
hg1868514
hg1768514
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517371
Supporting Variants
Samples
Known GenesATP6V1F, FLNC, KCP, LOC100130705
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666769
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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