A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6397621



Internal ID21055174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:56784486..56840071hg38UCSC Ensembl
chr6:56649284..56704869hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3855586
hg1955586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18146564
Samples
Known GenesDST
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6397621
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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