A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053311



Internal ID20620351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169538686..169539407hg38UCSC Ensembl
chr1:169507924..169508645hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323988
Supporting Variants
Samples
Known GenesF5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053311
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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