A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126609



Internal ID20693649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161719401..161721000hg38UCSC Ensembl
chr5:161146407..161148006hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411835
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00122


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