A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513751



Internal ID20887098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17121358..17123355hg38UCSC Ensembl
chr17:17024672..17026669hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034083
Samples
Known GenesMPRIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513751
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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