A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17608585



Internal ID21800632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95029197..95029252hg38UCSC Ensembl
chr13:95681451..95681506hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6033273
Supporting Variants
Samples
Known GenesABCC4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17608585
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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