A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406382



Internal ID21063935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73142761..73149642hg38UCSC Ensembl
chr6:73852484..73859365hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386882
hg196882
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147473
Samples
Known GenesKCNQ5, KCNQ5-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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