A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154010



Internal ID20721050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149105833..149107455hg38UCSC Ensembl
chr7:148802925..148804547hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381623
hg191623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421910
Supporting Variants
Samples
Known GenesZNF425
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154010
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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