A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528091



Internal ID20901452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78118276..78118576hg38UCSC Ensembl
chr17:76114357..76114657hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18038072
Samples
Known GenesTMC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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