A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18026257



Internal ID20593297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68285758..68286171hg38UCSC Ensembl
chr15:68578096..68578509hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503030
Supporting Variants
Samples
Known GenesFEM1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18026257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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