A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007158



Internal ID19096376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89896137..90091343hg38UCSC Ensembl
Innerchr2:89934947..90130185hg19UCSC Ensembl
Innerchr2:89571989..89767490hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38195207
hg19195239
hg18195502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3973n100
Supporting Variantsnssv3579810
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)nsv1007158
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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