A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062971



Internal ID20630011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75074452..75075109hg38UCSC Ensembl
chr1:75540136..75540793hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38658
hg19658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321089
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062971
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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