A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510884



Internal ID20884207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14928146..14934996hg38UCSC Ensembl
chr17:14831463..14838313hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg386851
hg196851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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