A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671598



Internal ID15408250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128832927..128908901hg38UCSC Ensembl
Innerchr7:128472981..128548954hg19UCSC Ensembl
Innerchr7:128260217..128336190hg18UCSC Ensembl
Innerchr7:128066932..128142905hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3875975
hg1975974
hg1875974
hg1775974
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)nssv671598
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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