A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009893



Internal ID19099112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141828336..141904547hg38UCSC Ensembl
Innerchr2:142585905..142662116hg19UCSC Ensembl
Innerchr2:142302375..142378586hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3876212
hg1976212
hg1876212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582813
Samples
Known GenesLRP1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009893
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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