A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1128359



Internal ID19262787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:110439210..110439266hg38UCSC Ensembl
Outerchr7:110079267..110079323hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3958667
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1128359
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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