A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324668



Internal ID20857796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158182997..158187569hg38UCSC Ensembl
chr1:158152787..158157359hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg384573
hg194573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052746
Samples
Known GenesCD1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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