A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18063184



Internal ID20630224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77053878..77056114hg38UCSC Ensembl
chr1:77519563..77521799hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg382237
hg192237
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331144
Supporting Variants
Samples
Known GenesST6GALNAC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18063184
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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