A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319012



Internal ID20852104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155567801..156556900hg38UCSC Ensembl
chr1:155537592..156526692hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38989100
hg19989101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200527
Samples
Known GenesARHGEF2, BGLAP, C1orf61, C1orf85, CCT3, DAP3, GON4L, IQGAP3, KIAA0907, LAMTOR2, LMNA, MEF2D, MEX3A, MIR6738, MIR7851, MIR9-1, MSTO1, MSTO2P, PAQR6, PMF1, PMF1-BGLAP, RAB25, RHBG, RIT1, RXFP4, SCARNA4, SEMA4A, SLC25A44, SMG5, SNORA42, SSR2, SYT11, TMEM79, TSACC, UBQLN4, VHLL, YY1AP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319012
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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