A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076987



Internal ID21986220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:151090961..151090961hg38UCSC Ensembl
chr3:150808748..150808748hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17553673
Samples
Known GenesMED12L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076987
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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