A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870790



Internal ID22645726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5191270..5192269hg38UCSC Ensembl
chr17:5094565..5095564hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475073
Samples
Known GenesLOC100130950, ZNF594
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870790
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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