A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398003



Internal ID21055556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72754801..72755700hg38UCSC Ensembl
chr6:73464524..73465423hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147450
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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