A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102682



Internal ID22011915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:871904..2377665hg38UCSC Ensembl
chr19:871904..2377663hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381505762
hg191505760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17627153
Samples
Known GenesABCA7, ABHD17A, ADAMTSL5, ADAT3, AMH, AP3D1, APC2, ARID3A, ATP5D, ATP8B3, BTBD2, C19orf24, C19orf25, C19orf26, C19orf35, CIRBP, CIRBP-AS1, CNN2, CSNK1G2, CSNK1G2-AS1, DAZAP1, DOT1L, EFNA2, GAMT, GPX4, GRIN3B, HMHA1, IZUMO4, JSRP1, KISS1R, KLF16, LINGO3, LOC100288123, LSM7, MBD3, MED16, MEX3D, MIDN, MIR1227, MIR1909, MIR4321, MIR6789, MKNK2, MOB3A, MUM1, NDUFS7, OAZ1, ONECUT3, PCSK4, PLEKHJ1, PLK5, POLR2E, R3HDM4, REEP6, REXO1, RPS15, SBNO2, SCAMP4, SF3A2, SPPL2B, STK11, TCF3, TMEM259, UQCR11, WDR18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102682
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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