A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2737408



Internal ID17837864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42913919..42921968hg38UCSC Ensembl
Innerchr9:66396588..66404638hg19UCSC Ensembl
Innerchr9:66136408..66144458hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg388050
hg198051
hg188051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969636
Supporting Variants
SamplesHGDP00998
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)nssv2737408
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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