A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005619



Internal ID19094836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88858087..89245848hg38UCSC Ensembl
Innerchr2:89157600..89545331hg19UCSC Ensembl
Innerchr2:88938715..89326446hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38387762
hg19387732
hg18387732
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3935n100
Supporting Variantsnssv3729823
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)nsv1005619
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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