A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504552



Internal ID20877814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32928329..32934808hg38UCSC Ensembl
chr17:31255347..31261826hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg386480
hg196480
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035592
Samples
Known GenesTMEM98
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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