A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521934



Internal ID20895295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76779718..76780648hg38UCSC Ensembl
chr17:74775800..74776730hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38931
hg19931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18037691
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521934
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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