A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010769



Internal ID19099986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:18824278..19236224hg38UCSC Ensembl
Innerchr2:19005544..19435985hg19UCSC Ensembl
Innerchr2:18869025..19299466hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38411947
hg19430442
hg18430442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3578980
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010769
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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