A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv973756



Internal ID18608971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:92888207..92893995hg38UCSC Ensembl
Innerchr9:95650489..95656277hg19UCSC Ensembl
Innerchr9:94690310..94696098hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg385789
hg195789
hg185789
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2753002, nssv2747269, nssv2751886, nssv2747968, nssv2749820, nssv2750434, nssv2753533, nssv2752062, nssv2749117, nssv2749579
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv973756
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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