A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118775



Internal ID18921563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:81891024..81891624hg38UCSC Ensembl
Outerchr17:79848900..79849500hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981086
SamplesKWS1
Known GenesALYREF
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118775
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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