A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153766



Internal ID20720806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40290429..40391124hg38UCSC Ensembl
chr7:40330028..40430723hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38100696
hg19100696
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6606084
Supporting Variants
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153766
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