A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6556663



Internal ID20929734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130198611..130199239hg38UCSC Ensembl
chr7:129838451..129839079hg19UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271737
Samples
Known GenesTMEM209
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6556663
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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