A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3959564



Internal ID19208753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:21290388..21351688hg38UCSC Ensembl
Outerchr17:21193700..21255000hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3861301
hg1961301
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1110294
Supporting Variants
SamplesKWS1
Known GenesMAP2K3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3959564
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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