A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951376



Internal ID16953563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98209789..98246288hg38UCSC Ensembl
Outerchr7:97839101..97875600hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3836500
hg1936500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998544
SamplesBILGI_BIOE
Known GenesBHLHA15, TECPR1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951376
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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