A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012570



Internal ID19101787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:88833599..89293986hg38UCSC Ensembl
Innerchr2:89133112..89593743hg19UCSC Ensembl
Innerchr2:88914227..89374858hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38460388
hg19460632
hg18460632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3933n100
Supporting Variantsnssv3728984
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)nsv1012570
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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