A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765072



Internal ID17484710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102507872..102522787hg38UCSC Ensembl
Innerchr11:102378603..102393518hg19UCSC Ensembl
Innerchr11:101883813..101898728hg18UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg3814916
hg1914916
hg1814916
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv972953
Supporting Variants
SamplesHGDP00998
Known GenesMMP7
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765072
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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