A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329956



Internal ID20863110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37640601..37656553hg38UCSC Ensembl
chr1:38106273..38122225hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3815953
hg1915953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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