A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965979



Internal ID18601209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:27367079..27371222hg38UCSC Ensembl
Innerchr21:28739398..28743541hg19UCSC Ensembl
Innerchr21:27661269..27665412hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384144
hg194144
hg184144
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2246450, nssv2246448, nssv2246443, nssv2246444, nssv2246449, nssv2246447, nssv2246446, nssv2246452, nssv2246445, nssv2246451
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR5009
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965979
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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