A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2743355



Internal ID17756974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:63977698..63979086hg38UCSC Ensembl
Innerchr9:69221118..69222512hg19UCSC Ensembl
Innerchr9:68510938..68512332hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg381389
hg191395
hg181395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv973707
Supporting Variants
SamplesHGDP00521
Known GenesCBWD6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2743355
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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