A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704588



Internal ID15441240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128837811..128920707hg38UCSC Ensembl
Innerchr7:128477865..128560761hg19UCSC Ensembl
Innerchr7:128265101..128347997hg18UCSC Ensembl
Innerchr7:128071816..128154712hg17UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3882897
hg1982897
hg1882897
hg1782897
Variant TypeCNV gain
Copy Number
Allele State
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)nssv704588
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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