A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4022480



Internal ID22084111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143521875..143870966hg38UCSC Ensembl
Outerchr7:143521765..143875073hg38UCSC Ensembl
Innerchr7:143218968..143568059hg19UCSC Ensembl
Outerchr7:143218858..143572166hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38353309
hg19353309
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156737
Supporting Variants
Samples
Known GenesCTAGE15, CTAGE6, EPHA1-AS1, FAM115A, FAM115C, LOC154761
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4022480
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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