A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007569



Internal ID19096788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87489228hg38UCSC Ensembl
Innerchr2:87373881..87788747hg19UCSC Ensembl
Innerchr2:87227392..87569862hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38342471
hg19414867
hg18342471
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3891n100
Supporting Variantsnssv3582256
Samples
Known GenesLINC00152, MIR4771-1, MIR4771-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007569
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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