A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218450



Internal ID20785490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140509496..140534188hg38UCSC Ensembl
chr7:140209296..140233988hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3824693
hg1924693
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416290
Supporting Variants
Samples
Known GenesDENND2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218450
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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