A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131846



Internal ID20698886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61964362..61972033hg38UCSC Ensembl
chr5:61260189..61267860hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg387672
hg197672
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6414442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131846
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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