A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057158



Internal ID20624198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207671368..207672936hg38UCSC Ensembl
chr1:207844713..207846281hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg381569
hg191569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327875
Supporting Variants
Samples
Known GenesCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057158
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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