A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068846



Internal ID21509438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132552127..132552183hg38UCSC Ensembl
chr10:134365631..134365687hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588528
Supporting Variants
SamplesNA20847
Known GenesINPP5A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068846
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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