A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231502



Internal ID20798542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139519301..139523500hg38UCSC Ensembl
chr7:139204047..139208246hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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