A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065195



Internal ID20632235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9258301..9269100hg38UCSC Ensembl
chr1:9318360..9329159hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3810800
hg1910800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334715
Supporting Variants
Samples
Known GenesH6PD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065195
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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