A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065113



Internal ID20632153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9111995..9113080hg38UCSC Ensembl
chr1:9172054..9173139hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg381086
hg191086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323288
Supporting Variants
Samples
Known GenesGPR157
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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