A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003435



Internal ID19092653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56398095..56430283hg38UCSC Ensembl
Innerchr2:56625230..56657418hg19UCSC Ensembl
Innerchr2:56478734..56510922hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3832189
hg1932189
hg1832189
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3576660
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)nsv1003435
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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