A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555767



Internal ID20928838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123743478..123744922hg38UCSC Ensembl
chr9:126505757..126507201hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg381445
hg191445
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18279808
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555767
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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