A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591088



Internal ID21539660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:7004262..7004320hg38UCSC Ensembl
chr17:6907581..6907639hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086688
SamplesHG00171
Known GenesALOX12, LOC100506713
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591088
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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