A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536739



Internal ID20910082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86344291..89254074hg38UCSC Ensembl
chr1:86809974..89719757hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg382909784
hg192909784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv255n223
Supporting Variantsnssv18251897
Samples
Known GenesCCBL2, CLCA1, CLCA2, CLCA3P, CLCA4, GBP1, GBP2, GBP3, GBP4, GBP7, GTF2B, HS2ST1, LINC01140, LMO4, LOC100505768, MIR7856, ODF2L, PKN2, RBMXL1, SEP15, SH3GLB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536739
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