A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083638



Internal ID21465101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60367167..60367216hg38UCSC Ensembl
chr15:60659366..60659415hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588899
Supporting Variants
SamplesHG03065
Known GenesANXA2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083638
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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