A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219685



Internal ID20786725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29651301..29742600hg38UCSC Ensembl
chr7:29690917..29782216hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3891300
hg1991300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617670
Supporting Variants
Samples
Known GenesDPY19L2P3, LOC646762, MIR550A3, ZNRF2P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219685
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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