A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122151



Internal ID18935450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:876363..878063hg38UCSC Ensembl
Outerchr7:916000..917700hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969591
SamplesKWS2
Known GenesGET4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122151
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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