A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18064100



Internal ID20631140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76226074..76258322hg38UCSC Ensembl
chr1:76691759..76724007hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3832249
hg1932249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330391
Supporting Variants
Samples
Known GenesST6GALNAC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18064100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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