A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603634



Internal ID21552299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15704730..15708948hg38UCSC Ensembl
chr17:15608044..15612262hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg384219
hg194219
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094625
SamplesHG03683
Known GenesZNF286A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603634
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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