A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002667



Internal ID18745199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15798074..15809279hg38UCSC Ensembl
Innerchr1:16124569..16135774hg19UCSC Ensembl
Innerchr1:15997156..16008361hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3811206
hg1911206
hg1811206
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3465075
Samples
Known GenesUQCRHL
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1002667
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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