A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697786



Internal ID15434438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1388817..1512784hg38UCSC Ensembl
Innerchr7:1428453..1552420hg19UCSC Ensembl
Innerchr7:1394979..1518946hg18UCSC Ensembl
Innerchr7:1201694..1325661hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38123968
hg19123968
hg18123968
hg17123968
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521100
Supporting Variants
Samples
Known GenesINTS1, MICALL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697786
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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