A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4765225



Internal ID20541085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1102251..1102251hg38UCSC Ensembl
chr10:1148191..1148191hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281160
Samples
Known GenesWDR37
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4765225
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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