A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729880



Internal ID19028161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88861741..89152659hg38UCSC Ensembl
Innerchr2:89161253..89452143hg19UCSC Ensembl
Innerchr2:88942368..89233258hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38290919
hg19290891
hg18290891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000244
Supporting Variants
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)nssv3729880
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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