A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904212



Internal ID3625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63922476..63924021hg38UCSC Ensembl
chr1:64388147..64389692hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg381546
hg191546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425135
Supporting Variants
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904212
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.004528


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