A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968614



Internal ID18603842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:36002593..36004093hg38UCSC Ensembl
Innerchr9:36002590..36004090hg19UCSC Ensembl
Innerchr9:35992590..35994090hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg381501
hg191501
hg181501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528601, nssv2528597, nssv2528604, nssv2528605, nssv2528599, nssv2528603, nssv2528606, nssv2528598, nssv2528600, nssv2528602
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)nsv968614
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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