A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052495



Internal ID19141714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55721419..55809966hg38UCSC Ensembl
Innerchr15:56013617..56102164hg19UCSC Ensembl
Innerchr15:53800909..53889456hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3888548
hg1988548
hg1888548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552446
Samples
Known GenesPRTG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052495
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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