A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407356



Internal ID21064909
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 StatusM
Merged Variants
Supporting Variantsnssv18215868
Samples
Known GenesHSPA4, ZCCHC10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407356
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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