A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518875



Internal ID15446168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1779543..1814627hg38UCSC Ensembl
Innerchr7:1819179..1854263hg19UCSC Ensembl
Innerchr7:1785705..1820789hg18UCSC Ensembl
Innerchr7:1592420..1627504hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3835085
hg1935085
hg1835085
hg1735085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696333
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518875
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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