A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065704



Internal ID20632744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9756969..9757482hg38UCSC Ensembl
chr1:9817027..9817540hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6326845
Supporting Variants
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065704
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00416


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