A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv976946



Internal ID18612152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:68833483..68835514hg38UCSC Ensembl
Innerchr15:69125822..69127853hg19UCSC Ensembl
Innerchr15:66912876..66914907hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382032
hg192032
hg182032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2029472, nssv2029470, nssv2029477, nssv2029469, nssv2029478, nssv2029473, nssv2029475, nssv2029471, nssv2029476, nssv2029474
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR548H4
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv976946
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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