A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150776



Internal ID20717816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141669797..141670109hg38UCSC Ensembl
chr7:141369597..141369909hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421918
Supporting Variants
Samples
Known GenesKIAA1147
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00275


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