A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969692



Internal ID18604919
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2756134, nssv2753322, nssv2754634, nssv2750104, nssv2756672, nssv2754403, nssv2755202, nssv2752807, nssv2754088, nssv2746977
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCBWD3
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969692
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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