A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002824



Internal ID19092041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208741026..208779609hg38UCSC Ensembl
Innerchr2:209605750..209644333hg19UCSC Ensembl
Innerchr2:209313995..209352578hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3838584
hg1938584
hg1838584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4161n100
Supporting Variantsnssv3585603, nssv3585604
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)nsv1002824
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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