A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17401018



Internal ID22458888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:72879065..72881466hg38UCSC Ensembl
chr2:73106194..73108595hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg382402
hg192402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17401018
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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