A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530488



Internal ID20903849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75287198..75287324hg38UCSC Ensembl
chr17:73283279..73283405hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037514
Samples
Known GenesSLC25A19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530488
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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