A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2719419



Internal ID17808202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74973701..74974354hg38UCSC Ensembl
Innerchr7:74387851..74388504hg19UCSC Ensembl
Innerchr7:74025787..74026440hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38654
hg19654
hg18654
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv970882
Supporting Variants
SamplesHGDP00778
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2719419
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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