A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518779



Internal ID15099386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:8016034..8037729hg38UCSC Ensembl
Innerchr7:8055664..8077359hg19UCSC Ensembl
Innerchr7:8022189..8043884hg18UCSC Ensembl
Innerchr7:7828904..7850599hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3821696
hg1921696
hg1821696
hg1721696
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696233
Samples
Known GenesGLCCI1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518779
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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