A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153605



Internal ID18852381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:55237640..55237727hg38UCSC Ensembl
Outerchr7:55305333..55305420hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002261
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153605
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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