A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119132



Internal ID19278904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:98281188..98281888hg38UCSC Ensembl
Outerchr7:97910500..97911200hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3623n106
Supporting Variantsnssv3981937
SamplesKWS1
Known GenesBRI3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119132
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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