A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131382



Internal ID20698422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63573698..63580464hg38UCSC Ensembl
chr5:62869525..62876291hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg386767
hg196767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6405165
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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