A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509344



Internal ID20882653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:14949934..14950622hg38UCSC Ensembl
chr17:14853251..14853939hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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