A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18156113



Internal ID20723153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:32502236..32503429hg38UCSC Ensembl
chr7:32541848..32543041hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381194
hg191194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616800
Supporting Variants
Samples
Known GenesAVL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18156113
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