A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6576038



Internal ID20949109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72631383..74206190hg38UCSC Ensembl
chr15:72923724..74498531hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381574808
hg191574808
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18241896
Samples
Known GenesADPGK, ADPGK-AS1, BBS4, C15orf59, C15orf60, CD276, GOLGA6A, GOLGA6B, HCN4, HIGD2B, ISLR, ISLR2, LOC283731, LOXL1, LOXL1-AS1, NEO1, NPTN, NPTN-IT1, PML, STOML1, STRA6, TBC1D21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6576038
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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