A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404157



Internal ID21061710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146032964..146035455hg38UCSC Ensembl
chr5:145412527..145415018hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382492
hg192492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126034
Samples
Known GenesSH3RF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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