A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232204



Internal ID20799244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105595689..105596309hg38UCSC Ensembl
chr7:105236136..105236756hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38621
hg19621
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600554
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232204
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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