A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231517



Internal ID20798557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:905578..987665hg38UCSC Ensembl
chr7:945215..1027301hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3882088
hg1982087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6609062
Supporting Variants
Samples
Known GenesADAP1, COX19, CYP2W1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231517
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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