A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011802



Internal ID18754336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9626042..9668155hg38UCSC Ensembl
Innerchr2:9766171..9808284hg19UCSC Ensembl
Innerchr2:9683622..9725735hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3842114
hg1942114
hg1842114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3726744
Samples
Known GenesYWHAQ
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011802
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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