A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333094



Internal ID20866269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:233637884..233642709hg38UCSC Ensembl
chr1:233773630..233778455hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059006
Samples
Known GenesKCNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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