A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2463273



Internal ID17752181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74969837..74973701hg38UCSC Ensembl
Innerchr7:74383987..74387851hg19UCSC Ensembl
Innerchr7:74021923..74025787hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383865
hg193865
hg183865
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv970534
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Commentslineage specific duplication - fixed_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2463273
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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