A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007803



Internal ID19097022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:185983043..186094561hg38UCSC Ensembl
Innerchr2:186847770..186959288hg19UCSC Ensembl
Innerchr2:186556015..186667533hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38111519
hg19111519
hg18111519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4131n100
Supporting Variantsnssv3583272, nssv3583273
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)nsv1007803
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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