A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv871849



Internal ID16165805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:42275938..42276943hg38UCSC Ensembl
Innerchr17:40427956..40428961hg19UCSC Ensembl
Innerchr17:37681482..37682487hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg381006
hg191006
hg181006
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575045
Supporting Variants
Samples
Known GenesSTAT5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv871849
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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