A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729965



Internal ID19028246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88903062..89198188hg38UCSC Ensembl
Innerchr2:89202578..89497676hg19UCSC Ensembl
Innerchr2:88983693..89278791hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38295127
hg19295099
hg18295099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv997604
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)nssv3729965
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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