A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578162



Internal ID20951233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69946889..70095387hg38UCSC Ensembl
chr10:71706645..71855143hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38148499
hg19148499
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234538
Samples
Known GenesCOL13A1, H2AFY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578162
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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