A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364032



Internal ID21021585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8949685..8981479hg38UCSC Ensembl
chr4:8951411..8983205hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3831795
hg1931795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5147n223
Supporting Variantsnssv18122474
Samples
Known GenesLOC650293
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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