A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv984092



Internal ID18272596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:75677911..75708346hg38UCSC Ensembl
Innerchr15:75970252..76000687hg19UCSC Ensembl
Innerchr15:73757307..73787742hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3830436
hg1930436
hg1830436
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2032019, nssv2032020, nssv2032024, nssv2032018, nssv2032022, nssv2032021, nssv2032025, nssv2032023, nssv2032016, nssv2032017
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCSPG4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv984092
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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