A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009324



Internal ID19098542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:91426526..91625195hg38UCSC Ensembl
Innerchr2:91618895..91813221hg19UCSC Ensembl
Innerchr2:90982622..91176948hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg38198670
hg19194327
hg18194327
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3990n100
Supporting Variantsnssv3579418, nssv3579417, nssv3729111, nssv3579419
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)nsv1009324
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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