A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009103



Internal ID19098321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146758..87588752hg38UCSC Ensembl
Innerchr2:87373881..87888271hg19UCSC Ensembl
Innerchr2:87227392..87669386hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38441995
hg19514391
hg18441995
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3892n100
Supporting Variantsnssv3582260, nssv3728735, nssv3728734
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)nsv1009103
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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