A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601003



Internal ID20974074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:95254993..95255353hg38UCSC Ensembl
chr7:94884305..94884665hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161615
Samples
Known GenesPPP1R9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601003
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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