A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2753776



Internal ID17727497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:65762114..65768709hg38UCSC Ensembl
Innerchr9:70397336..70403931hg19UCSC Ensembl
Innerchr9:69637156..69643751hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg386596
hg196596
hg186596
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv968697
Supporting Variants
SamplesHGDP00456
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2753776
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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