A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225181



Internal ID20792221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158361301..158916000hg38UCSC Ensembl
chr7:158153993..158708691hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38554700
hg19554699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417609
Supporting Variants
Samples
Known GenesESYT2, MIR5707, MIR595, NCAPG2, PTPRN2, WDR60
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225181
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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