A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065740



Internal ID20632780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9777076..9788083hg38UCSC Ensembl
chr1:9837134..9848141hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3811008
hg1911008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321990
Supporting Variants
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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