A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2756134



Internal ID17790078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:68282900..68283539hg38UCSC Ensembl
Innerchr9:70897816..70898455hg19UCSC Ensembl
Innerchr9:70087636..70088275hg18UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38640
hg19640
hg18640
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv969692
Supporting Variants
SamplesHGDP00665
Known GenesCBWD3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2756134
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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