A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062863



Internal ID20629903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71111388..71124187hg38UCSC Ensembl
chr1:71577071..71589870hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3812800
hg1912800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321336
Supporting Variants
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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