A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334684



Internal ID20867871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:210718314..210721196hg38UCSC Ensembl
chr1:210891656..210894538hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg382883
hg192883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057380
Samples
Known GenesKCNH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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