A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2719406



Internal ID17404477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74950172..74969837hg38UCSC Ensembl
Innerchr7:74365051..74383987hg19UCSC Ensembl
Innerchr7:74002987..74021923hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3819666
hg1918937
hg1818937
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv981529
Supporting Variants
SamplesHGDP00521
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Commentslineage specific expansions - expansion_Hsa-Hde
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2719406
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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