A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061994



Internal ID20629034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51528766..51532084hg38UCSC Ensembl
chr1:51994438..51997756hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg383319
hg193319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6318088
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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