A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614719



Internal ID20987790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:430997..434277hg38UCSC Ensembl
chr7:470980..474260hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg383281
hg193281
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217154
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614719
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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