A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519131



Internal ID20892492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78247001..78263000hg38UCSC Ensembl
chr17:76243082..76259081hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3816000
hg1916000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038091
Samples
Known GenesLOC100996291
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519131
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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