A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703562



Internal ID21225374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40601551..40601604hg38UCSC Ensembl
chr8:40459070..40459123hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816649
Supporting Variants
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703562
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.96875


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