A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007002



Internal ID19096220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89156379hg38UCSC Ensembl
Innerchr2:89133112..89455863hg19UCSC Ensembl
Innerchr2:88914227..89236978hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38322781
hg19322752
hg18322752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3926n100
Supporting Variantsnssv3728958
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)nsv1007002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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