A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6582161



Internal ID20955232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269745..86636480hg38UCSC Ensembl
chr14:77736088..87102824hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg389366736
hg199366737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18237512
Samples
Known GenesADCK1, AHSA1, ALKBH1, C14orf178, CEP128, DIO2, DIO2-AS1, FLRT2, GSTZ1, GTF2A1, ISM2, LINC00911, NGB, NOXRED1, NRXN3, POMT2, SAMD15, SEL1L, SLIRP, SNORA79, SNW1, SPTLC2, STON2, TMED8, TSHR, VIPAS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6582161
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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