A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3545669



Internal ID18497264
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 StatusS
Merged Variantsnsv1042783
Supporting Variants
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)nssv3545669
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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