A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149570



Internal ID18854182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:141411058..141411181hg38UCSC Ensembl
Outerchr7:141110858..141110981hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000872
SamplesKWB1
Known GenesTMEM178B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149570
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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