A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001141



Internal ID19090358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:139955277..140022363hg38UCSC Ensembl
Innerchr2:140712846..140779932hg19UCSC Ensembl
Innerchr2:140429316..140496402hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3867087
hg1967087
hg1867087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582805, nssv3729242
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)nsv1001141
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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