A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329595



Internal ID20862748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202061735..202069465hg38UCSC Ensembl
chr1:202030863..202038593hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg387731
hg197731
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056662
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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