A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577827



Internal ID20950898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:77269825..78082863hg38UCSC Ensembl
chr14:77736168..78549206hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38813039
hg19813039
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2210n223
Supporting Variantsnssv18237514
Samples
Known GenesADCK1, AHSA1, ALKBH1, C14orf178, GSTZ1, ISM2, NGB, NOXRED1, POMT2, SAMD15, SLIRP, SNW1, SPTLC2, TMED8, VIPAS39
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577827
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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