A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009717



Internal ID19098935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:51044124..51123977hg38UCSC Ensembl
Innerchr2:51271262..51351115hg19UCSC Ensembl
Innerchr2:51124766..51204619hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3879854
hg1979854
hg1879854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3814n100
Supporting Variantsnssv3581688, nssv3581689
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)nsv1009717
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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