A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071548



Internal ID21477640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:9273966..9274058hg38UCSC Ensembl
chr10:9315929..9316021hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593108
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071548
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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