A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948027



Internal ID18248187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:58212447..58214540hg38UCSC Ensembl
Innerchr10:59972208..59974301hg19UCSC Ensembl
Innerchr10:59642214..59644307hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg382094
hg192094
hg182094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1851356, nssv1851357, nssv1851353, nssv1851359, nssv1851354, nssv1851361, nssv1851358, nssv1851362, nssv1851355, nssv1851360
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesIPMK
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948027
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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