A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17071116



Internal ID21457656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:61667536..61667816hg38UCSC Ensembl
chr10:63427294..63427574hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588470
Supporting Variants
SamplesHG02587
Known GenesC10orf107
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17071116
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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