A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062990



Internal ID20630030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71841603..71872661hg38UCSC Ensembl
chr1:72307286..72338344hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3831059
hg1931059
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329253
Supporting Variants
Samples
Known GenesNEGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062990
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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