A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521414



Internal ID20894775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76450871..76464649hg38UCSC Ensembl
chr17:74446953..74460731hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3813779
hg1913779
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038230
Samples
Known GenesAANAT, UBE2O
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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