A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413342



Internal ID21070895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73392868..73399185hg38UCSC Ensembl
chr6:74102591..74108908hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386318
hg196318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147491
Samples
Known GenesDDX43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413342
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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