A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751024



Internal ID20526884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48923506..48923506hg38UCSC Ensembl
chr10:50131551..50131551hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16271225
Samples
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751024
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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