A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970196



Internal ID18605420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170736716..170745979hg38UCSC Ensembl
Innerchr6:171045804..171055000hg19UCSC Ensembl
Innerchr6:170887729..170897085hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg389264
hg199197
hg189357
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2433171, nssv2433170, nssv2433172, nssv2433177, nssv2433176, nssv2433175, nssv2433168, nssv2433173, nssv2433169, nssv2433174
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970196
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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