A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432563



Internal ID21394565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62788838..62790179hg38UCSC Ensembl
chr17:60866199..60867540hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg381342
hg191342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15750887
SamplesMDQ025
Known GenesMARCH10, MIR548W
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432563
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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