A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882352



Internal ID22657329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:42488288..42499189hg38UCSC Ensembl
chr17:40640306..40651207hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3810902
hg1910902
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17478246
Samples
Known GenesATP6V0A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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