A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951364



Internal ID16953551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:77406884..77415683hg38UCSC Ensembl
Outerchr7:77036201..77045000hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998533
SamplesBILGI_BIOE
Known GenesGSAP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951364
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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