A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973097



Internal ID18608312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:83150354..83152190hg38UCSC Ensembl
Innerchr12:83544133..83545969hg19UCSC Ensembl
Innerchr12:82068264..82070100hg18UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg381837
hg191837
hg181837
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1939346, nssv1939352, nssv1939353, nssv1939347, nssv1939345, nssv1939349, nssv1939350, nssv1939348, nssv1939351, nssv1939344
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)nsv973097
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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