A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405304



Internal ID21062857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4248671..4249170hg38UCSC Ensembl
chr6:4248905..4249404hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18143372
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405304
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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