A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051671



Internal ID20618711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114905101..114908523hg38UCSC Ensembl
chr1:115447722..115451144hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg383423
hg193423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327722
Supporting Variants
Samples
Known GenesSYCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051671
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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