A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893039



Internal ID22668096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132864618..132865161hg38UCSC Ensembl
chr5:132200310..132200853hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17418563
Samples
Known GenesGDF9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893039
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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