A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062239



Internal ID20629279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62806545..62807004hg38UCSC Ensembl
chr1:63272216..63272675hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335275
Supporting Variants
Samples
Known GenesATG4C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062239
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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