A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007376



Internal ID22069007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:224698790..224703338hg38UCSC Ensembl
Outerchr1:224698366..224706112hg38UCSC Ensembl
Innerchr1:224886492..224891040hg19UCSC Ensembl
Outerchr1:224886068..224893814hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg387747
hg197747
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154774
Supporting Variants
Samples
Known GenesCNIH3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007376
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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