A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728959



Internal ID19027240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89161550hg38UCSC Ensembl
Innerchr2:89133112..89461034hg19UCSC Ensembl
Innerchr2:88914227..89242149hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38327952
hg19327923
hg18327923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998817
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)nssv3728959
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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