A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538751



Internal ID20912065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:40447946..40449068hg38UCSC Ensembl
chr1:40913618..40914740hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg381123
hg191123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538751
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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