A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147440



Internal ID20714480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72687803..72697242hg38UCSC Ensembl
chr6:73397527..73406966hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg389440
hg199440
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403458
Supporting Variants
Samples
Known GenesKCNQ5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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