A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404332



Internal ID21061885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:12099295..12099819hg38UCSC Ensembl
chr6:12099528..12100052hg19UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg38525
hg19525
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18137300
Samples
Known GenesHIVEP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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