A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537952



Internal ID20911279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47906527..47907134hg38UCSC Ensembl
chr3:47948017..47948624hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4863n223
Supporting Variantsnssv18262103
Samples
Known GenesMAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537952
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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