A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556114



Internal ID20929185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140545424..140546340hg38UCSC Ensembl
chr7:140245224..140246140hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38917
hg19917
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18274455
Samples
Known GenesDENND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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