A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513591



Internal ID20886937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:9787580..9788683hg38UCSC Ensembl
chr17:9690897..9692000hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381104
hg191104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039168
Samples
Known GenesDHRS7C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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