A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6524093



Internal ID20897454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81210545..81212202hg38UCSC Ensembl
chr17:79184345..79186002hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381658
hg191658
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038528
Samples
Known GenesAZI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6524093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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