A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143851



Internal ID18929111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:31858881..31859481hg38UCSC Ensembl
Outerchr17:30185900..30186500hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994547
SamplesKWS1
Known GenesCOPRS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143851
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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