A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17370638



Internal ID22596307
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 StatusS
Merged Variantsnsv5944779
Supporting Variants
Samples
Known GenesBIRC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17370638
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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