A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503577



Internal ID20876832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36081063..36187381hg38UCSC Ensembl
chr17:34408421..34514757hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38106319
hg19106337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3093n223
Supporting Variantsnssv18035160
Samples
Known GenesCCL3, CCL4, TBC1D3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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