A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998011



Internal ID16944277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76443043..76450342hg38UCSC Ensembl
Outerchr10:78202801..78210100hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950979
Supporting Variants
SamplesBILGI_BIOE
Known GenesC10orf11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998011
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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