A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6547994



Internal ID20921193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109059516..109059858hg38UCSC Ensembl
chr1:109602138..109602480hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38343
hg19343
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6547994
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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