A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052943



Internal ID20619983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150117317..150119850hg38UCSC Ensembl
chr1:150089435..150091968hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg382534
hg192534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321156
Supporting Variants
Samples
Known GenesVPS45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052943
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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