A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113850



Internal ID19274376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:11210703..11210769hg38UCSC Ensembl
Outerchr17:11114020..11114086hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969925
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113850
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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