A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118772



Internal ID19263892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:79466318..79512418hg38UCSC Ensembl
Outerchr17:77462400..77508500hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3846101
hg1946101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981082
SamplesKWS1
Known GenesRBFOX3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118772
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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