A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052447



Internal ID20619487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:160165529..160166042hg38UCSC Ensembl
chr1:160135319..160135832hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322144
Supporting Variants
Samples
Known GenesATP1A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052447
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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