A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126281



Internal ID20693321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136573801..136576700hg38UCSC Ensembl
chr5:135909490..135912389hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412124
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126281
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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