A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215868



Internal ID20782908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:133013138..133059328hg38UCSC Ensembl
chr5:132348830..132395020hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3846191
hg1946191
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407356
Supporting Variants
Samples
Known GenesHSPA4, ZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215868
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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