A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3945916



Internal ID21365985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101976000..101976000hg38UCSC Ensembl
chr10:103735757..103735757hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15191702
SamplesHG002
Known GenesC10orf76
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3945916
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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