A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062576



Internal ID20629616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71820144..71820807hg38UCSC Ensembl
chr1:72285827..72286490hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38664
hg19664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319882
Supporting Variants
Samples
Known GenesNEGR1, NEGR1-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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