A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6383602



Internal ID21041155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17009016..17138657hg38UCSC Ensembl
chr5:17009125..17138766hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38129642
hg19129642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129600
Samples
Known GenesLOC285696
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6383602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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