A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060459



Internal ID20627499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32465061..32475410hg38UCSC Ensembl
chr1:32930662..32941011hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg3810350
hg1910350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316401
Supporting Variants
Samples
Known GenesZBTB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060459
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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