A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397673



Internal ID21055226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77433793..77434149hg38UCSC Ensembl
chr6:78143510..78143866hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148307
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397673
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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