A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025727



Internal ID20592767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75497086..75501758hg38UCSC Ensembl
chr15:75789427..75794099hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg384673
hg194673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502207
Supporting Variants
Samples
Known GenesPTPN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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