A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704562



Internal ID15094528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12496710..12579139hg38UCSC Ensembl
Innerchr7:12536336..12618764hg19UCSC Ensembl
Innerchr7:12502861..12585289hg18UCSC Ensembl
Innerchr7:12309576..12392004hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3882430
hg1982429
hg1882429
hg1782429
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528031
Supporting Variants
Samples
Known GenesSCIN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704562
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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