A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515197



Internal ID20888556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:44379121..44379417hg38UCSC Ensembl
chr17:42456489..42456785hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035843
Samples
Known GenesITGA2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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