A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6580180



Internal ID20953251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:32820867..32869684hg38UCSC Ensembl
chr10:33109795..33158612hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3848818
hg1948818
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232014
Samples
Known GenesCCDC7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6580180
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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