A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv974953



Internal ID18610162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:125903196..125905620hg38UCSC Ensembl
Innerchr10:127591765..127594189hg19UCSC Ensembl
Innerchr10:127581755..127584179hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382425
hg192425
hg182425
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2616302, nssv2616299, nssv2616297, nssv2616301, nssv2616303, nssv2616306, nssv2616304, nssv2616298, nssv2616300, nssv2616305
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFANK1
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv974953
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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