A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972663



Internal ID18607879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34832418..34835516hg38UCSC Ensembl
Innerchr9:34832415..34835513hg19UCSC Ensembl
Innerchr9:34822415..34825513hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg383099
hg193099
hg183099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528382, nssv2528380, nssv2528379, nssv2528378, nssv2528381, nssv2528385, nssv2528383, nssv2528377, nssv2528384, nssv2528386
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM205B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972663
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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