A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010787



Internal ID19100004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90144550hg38UCSC Ensembl
Innerchr2:89934947..90183404hg19UCSC Ensembl
Innerchr2:89571989..89820709hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38248414
hg19248458
hg18248721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3975n100
Supporting Variantsnssv3579811
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)nsv1010787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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