A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2340780



Internal ID17776611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:165258596..165276381hg38UCSC Ensembl
Innerchr4:166179748..166197533hg19UCSC Ensembl
Innerchr4:166399198..166416983hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3817786
hg1917786
hg1817786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv980272
Supporting Variants
SamplesHGDP00542
Known GenesKLHL2
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)nssv2340780
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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