A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089604



Internal ID20656644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71379738..71380063hg38UCSC Ensembl
chr2:71606868..71607193hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345572
Supporting Variants
Samples
Known GenesZNF638
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00193


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