A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572498



Internal ID20945569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75704918..77511682hg38UCSC Ensembl
chr7:75334236..77140999hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381806765
hg191806764
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18276554
Samples
Known GenesCCDC146, CCL24, CCL26, DTX2, DTX2P1-UPK3BP1-PMS2P11, FDPSP2, FGL2, GSAP, HIP1, HSPB1, LOC100132832, LOC100133091, MDH2, MIR4651, POMZP3, POR, RHBDD2, SNORA14A, SRCRB4D, SRRM3, STYXL1, TMEM120A, UPK3B, YWHAG, ZP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572498
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer