A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156354



Internal ID22084830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:80265186..80955858hg38UCSC Ensembl
Outerchr5:80260241..80961090hg38UCSC Ensembl
Innerchr5:79561005..80251677hg19UCSC Ensembl
Outerchr5:79556060..80256909hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg38700850
hg19700850
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018791
Samples
Known GenesANKRD34B, CRSP8P, DHFR, FAM151B, LOC102524628, LOC644936, MSH3, MTRNR2L2, RASGRF2, SPZ1, ZFYVE16
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156354
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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