A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578547



Internal ID20951618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104070004..110020477hg38UCSC Ensembl
chr11:103940732..109891203hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg385950474
hg195950472
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221435
Samples
Known GenesAASDHPPT, ACAT1, ALKBH8, ATM, C11orf65, C11orf87, CARD16, CARD17, CARD18, CASP1, CASP12, CASP4, CASP5, CUL5, CWF19L2, DDX10, ELMOD1, EXPH5, GRIA4, GUCY1A2, KBTBD3, KDELC2, LOC643733, LOC643923, MSANTD4, NPAT, PDGFD, RAB39A, SLC35F2, SLN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578547
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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