A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152857



Internal ID19197611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156133480..156133587hg38UCSC Ensembl
Outerchr7:155926174..155926281hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997889
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152857
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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