A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141303



Internal ID19269313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:21290388..21351288hg38UCSC Ensembl
Outerchr17:21193700..21254600hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3860901
hg1960901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1433n106
Supporting Variantsnssv3992808
SamplesKWS2
Known GenesMAP2K3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141303
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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