A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042783



Internal ID18785314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28110984..28203495hg38UCSC Ensembl
Innerchr15:28356130..28448641hg19UCSC Ensembl
Innerchr15:26029725..26122236hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3892512
hg1992512
hg1892512
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2490n100
Supporting Variantsnssv3545669, nssv3545668
Samples
Known GenesHERC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042783
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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