A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540463



Internal ID20913755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155170892..155171365hg38UCSC Ensembl
chr1:155143368..155143841hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247107
Samples
Known GenesKRTCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540463
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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