A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011179



Internal ID19100396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89314751hg38UCSC Ensembl
Innerchr2:89133112..89614508hg19UCSC Ensembl
Innerchr2:88914227..89395623hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38481153
hg19481397
hg18481397
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n100
Supporting Variantsnssv3728985
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011179
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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