A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1840402



Internal ID17431424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38013010..38017473hg38UCSC Ensembl
Innerchr10:38301938..38306401hg19UCSC Ensembl
Innerchr10:38341944..38346407hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg384464
hg194464
hg184464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv947853
Supporting Variants
SamplesHGDP00665
Known GenesZNF33A
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)nssv1840402
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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