A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001676



Internal ID19090893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:52028097..52084529hg38UCSC Ensembl
Innerchr2:52255235..52311667hg19UCSC Ensembl
Innerchr2:52108739..52165171hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3856433
hg1956433
hg1856433
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581696
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)nsv1001676
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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