A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982763



Internal ID18617958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:48010946..48016980hg38UCSC Ensembl
Innerchr10:49218971..49224996hg19UCSC Ensembl
Innerchr10:48888977..48895002hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg386035
hg196026
hg186026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2613873, nssv2613878, nssv2613872, nssv2613875, nssv2613880, nssv2613876, nssv2613874, nssv2613877, nssv2613879, nssv2613881
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCTGLF12P
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982763
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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