A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729776



Internal ID19028057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88844243..89011844hg38UCSC Ensembl
Innerchr2:89143756..89311341hg19UCSC Ensembl
Innerchr2:88924871..89092456hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38167602
hg19167586
hg18167586
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012750
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)nssv3729776
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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