A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6534265



Internal ID20907626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76734038..76743570hg38UCSC Ensembl
chr17:74730120..74739652hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389533
hg199533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037727
Samples
Known GenesMFSD11, MIR636, SRSF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6534265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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