A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412404



Internal ID21069957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:44847396..44848137hg38UCSC Ensembl
chr6:44815133..44815874hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38742
hg19742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144099
Samples
Known GenesSUPT3H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412404
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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