A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965717



Internal ID18600947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35469687..35470884hg38UCSC Ensembl
Innerchr6:35437464..35438661hg19UCSC Ensembl
Innerchr6:35545442..35546639hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381198
hg191198
hg181198
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2406392, nssv2406399, nssv2406398, nssv2406397, nssv2406393, nssv2406396, nssv2406391, nssv2406395, nssv2406394, nssv2406400
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR7111, RPL10A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965717
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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