A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327858



Internal ID20861001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155271518..155272343hg38UCSC Ensembl
chr1:155241309..155242134hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38826
hg19826
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052065
Samples
Known GenesCLK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327858
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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