A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2538977



Internal ID17752527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42807809..42831967hg38UCSC Ensembl
Innerchr9:44139152..44163310hg19UCSC Ensembl
Innerchr9:44079148..44103306hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3824159
hg1924159
hg1824159
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv982249
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2538977
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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