A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535992



Internal ID20909346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61809865..61810694hg38UCSC Ensembl
chr1:62275537..62276366hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38830
hg19830
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250496
Samples
Known GenesINADL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535992
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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