A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334357



Internal ID20867542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11314524..11317575hg38UCSC Ensembl
chr1:11374581..11377632hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383052
hg193052
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18051371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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