A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007743



Internal ID19096962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89200973hg38UCSC Ensembl
Innerchr2:89133112..89500461hg19UCSC Ensembl
Innerchr2:88914227..89281576hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38367375
hg19367350
hg18367350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3926n100
Supporting Variantsnssv3728965
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)nsv1007743
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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