A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036994



Internal ID19126213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:60229106..60257654hg38UCSC Ensembl
Innerchr15:60521305..60549853hg19UCSC Ensembl
Innerchr15:58308597..58337145hg18UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3828549
hg1928549
hg1828549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2611n100
Supporting Variantsnssv3553620
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)nsv1036994
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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