A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326223



Internal ID20859357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159849053..159897513hg38UCSC Ensembl
chr1:159818843..159867303hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3848461
hg1948461
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052426
Samples
Known GenesC1orf204, CCDC19, VSIG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326223
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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