A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106164



Internal ID20673204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:101654187..102010070hg38UCSC Ensembl
chr4:102575344..102931227hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38355884
hg19355884
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377164
Supporting Variants
Samples
Known GenesBANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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