A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577000



Internal ID20950071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28174418..30818114hg38UCSC Ensembl
chr15:28419564..31110317hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg382643697
hg192690754
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2469n223
Supporting Variantsnssv18239428
Samples
Known GenesAPBA2, ARHGAP11B, CHRFAM7A, DKFZP434L187, FAM189A1, GOLGA6L7P, GOLGA8F, GOLGA8G, GOLGA8H, GOLGA8J, GOLGA8M, GOLGA8T, HERC2, HERC2P10, HERC2P9, LOC100288637, LOC100289656, LOC101059918, LOC646278, MIR4509-1, MIR4509-2, MIR4509-3, NDNL2, TJP1, ULK4P1, ULK4P2, ULK4P3, WHAMMP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577000
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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