A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532761



Internal ID20906122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55726708..55727090hg38UCSC Ensembl
chr17:53804069..53804451hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036950
Samples
Known GenesTMEM100
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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