A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932819



Internal ID22708123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76082936..76082991hg38UCSC Ensembl
chr17:74079017..74079072hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17375601
Samples
Known GenesEXOC7
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932819
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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