A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380643



Internal ID21038196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:176025949..176130576hg38UCSC Ensembl
chr4:176947100..177051727hg19UCSC Ensembl
Cytoband4q34.2
Allele length
AssemblyAllele length
hg38104628
hg19104628
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113590
Samples
Known GenesWDR17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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