A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5939106



Internal ID22714495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38008106..40186655hg38UCSC Ensembl
chr15:38300307..40478856hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382178550
hg192178550
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387554
Samples
Known GenesBMF, BUB1B, C15orf53, C15orf54, EIF2AK4, FAM98B, FSIP1, GPR176, RASGRP1, SPRED1, SRP14, SRP14-AS1, THBS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5939106
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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