A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525152



Internal ID20898513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:55094860..55095605hg38UCSC Ensembl
chr17:53172221..53172966hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18036906
Samples
Known GenesSTXBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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