A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050350



Internal ID20617390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10460953..10468840hg38UCSC Ensembl
chr1:10521010..10528897hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387888
hg197888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329736
Supporting Variants
Samples
Known GenesDFFA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050350
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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