A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728798



Internal ID19027079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88824623..90282526hg38UCSC Ensembl
Innerchr2:89124136..90321385hg19UCSC Ensembl
Innerchr2:88905251..89958690hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381457904
hg191197250
hg181053440
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000009
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)nssv3728798
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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