A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6620018



Internal ID20993089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14974501..14996200hg38UCSC Ensembl
chr7:15014126..15035825hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3821700
hg1921700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6594n223
Supporting Variantsnssv18228078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6620018
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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