A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062929



Internal ID20629969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71633106..71634030hg38UCSC Ensembl
chr1:72098789..72099713hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38925
hg19925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332496
Supporting Variants
Samples
Known GenesNEGR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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