A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013892



Internal ID19103111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51875532..52036093hg38UCSC Ensembl
Innerchr2:52102670..52263231hg19UCSC Ensembl
Innerchr2:51956174..52116735hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg38160562
hg19160562
hg18160562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3816n100
Supporting Variantsnssv3726029
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)nsv1013892
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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