A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv949951



Internal ID16952138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:134128848..134129647hg38UCSC Ensembl
Outerchr7:133813601..133814400hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998592
SamplesBILGI_BIOE
Known GenesLRGUK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv949951
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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