A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577345



Internal ID20950416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77012562..77945687hg38UCSC Ensembl
chr14:77478905..78412030hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38933126
hg19933126
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2210n223
Supporting Variantsnssv18237506
Samples
Known GenesADCK1, AHSA1, ALKBH1, C14orf178, GSTZ1, IRF2BPL, ISM2, KIAA1737, MIR1260A, NGB, NOXRED1, POMT2, SAMD15, SLIRP, SNW1, SPTLC2, TMED8, TMEM63C, VIPAS39, ZDHHC22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577345
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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