A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153112



Internal ID20720152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144496001..144497300hg38UCSC Ensembl
chr7:144193094..144194393hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428099
Supporting Variants
Samples
Known GenesTPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153112
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00047


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