A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17397637



Internal ID22455507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213172121..213172417hg38UCSC Ensembl
chr2:214036845..214037141hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906128
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17397637
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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