A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6541523



Internal ID20914805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6341339..6341543hg38UCSC Ensembl
chr1:6401399..6401603hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38205
hg19205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250593
Samples
Known GenesACOT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6541523
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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