A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539657



Internal ID20912953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112546178..112547388hg38UCSC Ensembl
chr1:113088800..113090010hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247417
Samples
Known GenesST7L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539657
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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