A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014616



Internal ID19103834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:38758330..38795751hg38UCSC Ensembl
Innerchr2:38985472..39022893hg19UCSC Ensembl
Innerchr2:38838976..38876397hg18UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3837422
hg1937422
hg1837422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3581475
Samples
Known GenesGEMIN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014616
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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