A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17398172



Internal ID22456042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38755999..38756078hg38UCSC Ensembl
chr2:38983141..38983220hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5877159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17398172
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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