A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930690



Internal ID22705961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:36923348..36923437hg38UCSC Ensembl
chr17:35280632..35280721hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17387091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930690
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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