A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413039



Internal ID21070592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82953300..82957453hg38UCSC Ensembl
chr5:82249119..82253272hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg384154
hg194154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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