A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17392602



Internal ID22450472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:5156060..5156181hg38UCSC Ensembl
chr2:5296193..5296314hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5873469
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17392602
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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