A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997522



Internal ID18810372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16961924..17126113hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg18164190
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv101n100
Supporting Variantsnssv3463781
Samples
Known GenesCROCC, MIR3675, MST1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997522
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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