A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18275629



Internal ID20842669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36908000..36952892hg38UCSC Ensembl
chr7:36947605..36992498hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3844893
hg1944894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6575054
Supporting Variants
Samples
Known GenesELMO1, MIR1200
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18275629
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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