A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062693



Internal ID20629733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67814389..67830300hg38UCSC Ensembl
chr1:68280072..68295983hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3815912
hg1915912
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317550
Supporting Variants
Samples
Known GenesGNG12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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