A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330050



Internal ID20863204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:216868801..216872100hg38UCSC Ensembl
chr1:217042143..217045442hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057555
Samples
Known GenesESRRG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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