A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17067404



Internal ID21505900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101025579..101025778hg38UCSC Ensembl
chr10:102785336..102785535hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38200
hg19200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596943
Supporting Variants
SamplesNA19983
Known GenesPDZD7
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17067404
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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