A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2544607



Internal ID17806239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62690251..62709729hg38UCSC Ensembl
Innerchr9:47001552..47021030hg19UCSC Ensembl
Innerchr9:46841372..46860850hg18UCSC Ensembl
Cytoband9p11.1
Allele length
AssemblyAllele length
hg3819479
hg1919479
hg1819479
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv968670
Supporting Variants
SamplesHGDP00778
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)nssv2544607
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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