A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131707



Internal ID20698747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:54707099..54712711hg38UCSC Ensembl
chr5:54002927..54008539hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg385613
hg195613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399205
Supporting Variants
Samples
Known GenesLOC102467080
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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