A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5596724



Internal ID21545333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:61914428..61915066hg38UCSC Ensembl
chr17:59991789..59992427hg19UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091236
SamplesHG00864
Known GenesINTS2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5596724
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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