A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666837



Internal ID15056803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:34859623..34868174hg38UCSC Ensembl
Innerchr7:34899235..34907786hg19UCSC Ensembl
Innerchr7:34865760..34874311hg18UCSC Ensembl
Innerchr7:34672475..34681026hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg388552
hg198552
hg188552
hg178552
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516166
Supporting Variants
Samples
Known GenesNPSR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666837
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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