A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590311



Internal ID20963382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:16144251..19584623hg38UCSC Ensembl
chr11:16165797..19606170hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg383440373
hg193440374
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224923
Samples
Known GenesABCC8, C11orf58, CSRP3, E2F8, GTF2H1, HPS5, IGSF22, KCNC1, KCNJ11, LDHA, LDHAL6A, LDHC, LOC494141, MIR4486, MRGPRX1, MRGPRX2, MRGPRX3, MRGPRX4, MYOD1, NAV2, NAV2-AS4, NAV2-AS5, NCR3LG1, NUCB2, OR7E14P, OTOG, PIK3C2A, PLEKHA7, PTPN5, RPS13, SAA1, SAA2, SAA2-SAA4, SAA3P, SAA4, SAAL1, SERGEF, SOX6, SPTY2D1, SPTY2D1-AS1, TMEM86A, TPH1, TSG101, UEVLD, USH1C, ZDHHC13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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