A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970808



Internal ID18606030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27326621..27329596hg38UCSC Ensembl
Innerchr7:27366240..27369215hg19UCSC Ensembl
Innerchr7:27332765..27335740hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg382976
hg192976
hg182976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2440237, nssv2440235, nssv2440233, nssv2440231, nssv2440229, nssv2440230, nssv2440234, nssv2440236, nssv2440232, nssv2440228
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970808
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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