A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510484



Internal ID20883803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:21153560..21166554hg38UCSC Ensembl
chr17:21056873..21069867hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3812995
hg1912995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18034296
Samples
Known GenesDHRS7B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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