A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398791



Internal ID21056344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1829184..1832771hg38UCSC Ensembl
chr6:1829418..1833005hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg383588
hg193588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143051
Samples
Known GenesGMDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398791
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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