A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395863



Internal ID21053416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168461272..168461944hg38UCSC Ensembl
chr5:167888277..167888949hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38673
hg19673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129527
Samples
Known GenesWWC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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