A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564472



Internal ID20937543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140579039..140579570hg38UCSC Ensembl
chr7:140278839..140279370hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38532
hg19532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274457
Samples
Known GenesDENND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564472
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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