A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112921



Internal ID19270415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:1664564..1674164hg38UCSC Ensembl
Outerchr7:1704200..1713800hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg389601
hg199601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967423
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112921
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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