A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005801



Internal ID20572841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93102074..93114275hg38UCSC Ensembl
chr12:93495850..93508051hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3812202
hg1912202
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6472703
Supporting Variants
Samples
Known GenesLOC643339
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005801
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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