A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947749



Internal ID18594596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15170248..15172688hg38UCSC Ensembl
Innerchr10:15212247..15214687hg19UCSC Ensembl
Innerchr10:15252253..15254693hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382441
hg192441
hg182441
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1833217, nssv1833214, nssv1833212, nssv1833211, nssv1833218, nssv1833210, nssv1833215, nssv1833213, nssv1833216, nssv1833219
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947749
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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