A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052078



Internal ID20619118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155500960..155506819hg38UCSC Ensembl
chr1:155470751..155476610hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg385860
hg195860
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322247
Supporting Variants
Samples
Known GenesASH1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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