A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944779



Internal ID22720248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78217308..78218077hg38UCSC Ensembl
chr17:76213389..76214158hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38770
hg19770
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370638
Samples
Known GenesBIRC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944779
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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