A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974618



Internal ID18263143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85379452..85384895hg38UCSC Ensembl
Innerchr15:85922683..85928126hg19UCSC Ensembl
Innerchr15:83723687..83729130hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg385444
hg195444
hg185444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2035895, nssv2035889, nssv2035891, nssv2035897, nssv2035894, nssv2035896, nssv2035888, nssv2035892, nssv2035890, nssv2035893
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAKAP13
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974618
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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