A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948202



Internal ID18595048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:118871107..118873399hg38UCSC Ensembl
Innerchr10:120630619..120632911hg19UCSC Ensembl
Innerchr10:120620609..120622901hg18UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382293
hg192293
hg182293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866962, nssv1866964, nssv1866965, nssv1866968, nssv1866966, nssv1866970, nssv1866969, nssv1866971, nssv1866967, nssv1866963
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)nsv948202
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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