A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981175



Internal ID18616374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112616125..112617807hg38UCSC Ensembl
Innerchr6:112937327..112939009hg19UCSC Ensembl
Innerchr6:113044020..113045702hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg381683
hg191683
hg181683
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2420599, nssv2420607, nssv2420603, nssv2420605, nssv2420601, nssv2420598, nssv2420604, nssv2420606, nssv2420602, nssv2420600
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)nsv981175
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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