A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317800



Internal ID20850889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23369600..23372754hg38UCSC Ensembl
chr1:23696093..23699247hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383155
hg193155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059010
Samples
Known GenesC1orf213, ZNF436
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317800
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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