A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535678



Internal ID20849138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:42780540..42790764hg38UCSC Ensembl
chr1:43246211..43256435hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg3810225
hg1910225
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18250986
Samples
Known GenesLOC100129924
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535678
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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