A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499263



Internal ID20872481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:30460416..30460909hg38UCSC Ensembl
chr17:28787434..28787927hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38494
hg19494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18035377
Samples
Known GenesCPD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499263
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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