A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696552



Internal ID15433204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31094703..31096996hg38UCSC Ensembl
Innerchr7:31134317..31136610hg19UCSC Ensembl
Innerchr7:31100842..31103135hg18UCSC Ensembl
Innerchr7:30907557..30909850hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg382294
hg192294
hg182294
hg172294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519081
Supporting Variants
Samples
Known GenesADCYAP1R1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696552
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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