A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519689



Internal ID20893050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75883686..75922197hg38UCSC Ensembl
chr17:73879767..73918278hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3838512
hg1938512
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038174
Samples
Known GenesFBF1, MRPL38, TRIM65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519689
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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