A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6566770



Internal ID20939841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42194666..44186502hg38UCSC Ensembl
chr6:42162404..44154239hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381991837
hg191991836
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18271282
Samples
Known GenesABCC10, ATP6V0CP3, C6orf223, C6orf226, CAPN11, CNPY3, CRIP3, CUL7, CUL9, DLK2, DNPH1, GLTSCR1L, GNMT, GTPBP2, GUCA1B, KLC4, KLHDC3, LOC100132354, LRRC73, MAD2L1BP, MEA1, MIR6780B, MRPL14, MRPL2, MRPS10, MRPS18A, PEX6, POLH, POLR1C, PPP2R5D, PRPH2, PTCRA, PTK7, RPL7L1, RRP36, RSPH9, SLC22A7, SRF, TBCC, TJAP1, TMEM63B, TRERF1, TTBK1, UBR2, VEGFA, XPO5, YIPF3, ZNF318
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6566770
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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