A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2523018



Internal ID17812749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15579329..15590305hg38UCSC Ensembl
Innerchr9:15579327..15590303hg19UCSC Ensembl
Innerchr9:15569327..15580303hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3810977
hg1910977
hg1810977
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv982197
Supporting Variants
SamplesHGDP00927
Known GenesCCDC171
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Pab-Ppy-Ggod-Ggog-Gbeg-Ptrs-Ptrt-Ptre-Ptrv-Ppa-Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2523018
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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