A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020010



Internal ID19109229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:159108175..159198763hg38UCSC Ensembl
Innerchr7:158900866..158991452hg19UCSC Ensembl
Innerchr7:158593627..158684213hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3890589
hg1990587
hg1890587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757755
Samples
Known GenesVIPR2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020010
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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