A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18025464



Internal ID20592504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67575901..67577600hg38UCSC Ensembl
chr15:67868239..67869938hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510835
Supporting Variants
Samples
Known GenesMAP2K5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18025464
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0336


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