A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152310



Internal ID20719350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16603553..16608654hg38UCSC Ensembl
chr7:16643178..16648279hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601808
Supporting Variants
Samples
Known GenesANKMY2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152310
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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