A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729802



Internal ID19028083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88848330..89245848hg38UCSC Ensembl
Innerchr2:89147843..89545331hg19UCSC Ensembl
Innerchr2:88928958..89326446hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38397519
hg19397489
hg18397489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1001098
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)nssv3729802
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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