A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402931



Internal ID21060484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72043501..72044300hg38UCSC Ensembl
chr6:72753204..72754003hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147371
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402931
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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