A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003307



Internal ID19190387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:134665248..134665664hg38UCSC Ensembl
Outerchr7:134350000..134350416hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38417
hg19417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154035
Supporting Variants
SamplesKWB1
Known GenesBPGM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003307
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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