A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007434



Internal ID19096653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87260810..87725136hg38UCSC Ensembl
Innerchr2:87487933..88024655hg19UCSC Ensembl
Innerchr2:87341444..87805770hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38464327
hg19536723
hg18464327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3899n100
Supporting Variantsnssv3728787
Samples
Known GenesLINC00152, MIR4435-1, MIR4435-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007434
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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