A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927855



Internal ID22703087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3618543..3631080hg38UCSC Ensembl
chr17:3521837..3534374hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3812538
hg1912538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373883
Samples
Known GenesSHPK
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927855
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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