A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543553



Internal ID20916799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156166229..156166739hg38UCSC Ensembl
chr1:156136020..156136530hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38511
hg19511
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247152
Samples
Known GenesSEMA4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543553
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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