A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101443



Internal ID20668483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48602284..48616913hg38UCSC Ensembl
chr3:48639717..48654346hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3814630
hg1914630
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355776
Supporting Variants
Samples
Known GenesUQCRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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