A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415295



Internal ID21072848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132864618..132865162hg38UCSC Ensembl
chr5:132200310..132200854hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215864
Samples
Known GenesGDF9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415295
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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