A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061949



Internal ID20628989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:59272287..59272709hg38UCSC Ensembl
chr1:59737959..59738381hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321653
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00048


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