A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582485



Internal ID20955556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:100023537..103679304hg38UCSC Ensembl
chr11:99894269..103550032hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383655768
hg193655764
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223549
Samples
Known GenesANGPTL5, ARHGAP42, BIRC2, BIRC3, C11orf70, CNTN5, DCUN1D5, DYNC2H1, KIAA1377, LOC101054525, MIR3920, MMP1, MMP10, MMP12, MMP13, MMP20, MMP27, MMP3, MMP7, MMP8, PGR, TMEM123, TMEM133, TRPC6, WTAPP1, YAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582485
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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