A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396442



Internal ID21053995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54600401..54602500hg38UCSC Ensembl
chr6:54465199..54467298hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18144778
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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