A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5876022



Internal ID22650982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61783294..61784593hg38UCSC Ensembl
chr17:59860655..59861954hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475749
Samples
Known GenesBRIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5876022
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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