A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6599358



Internal ID20972429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10362749..19023339hg38UCSC Ensembl
chr20:10343397..19003983hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg388660591
hg198660587
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18252841
Samples
Known GenesBANF2, BFSP1, BTBD3, C20orf78, CSRP2BP, DSTN, DTD1, DZANK1, ESF1, FLRT3, ISM1, ISM1-AS1, JAG1, KIF16B, LINC00493, LINC00652, LINC00851, LOC100270804, LOC339593, MACROD2, MACROD2-AS1, MACROD2-IT1, MGME1, MIR3192, MIR6870, MKKS, NDUFAF5, OTOR, OVOL2, PCSK2, PET117, POLR3F, RBBP9, RRBP1, SCP2D1, SEC23B, SEL1L2, SLX4IP, SNORD17, SNRPB2, SNX5, SPTLC3, TASP1, ZNF133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6599358
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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