A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002153



Internal ID19091370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:78614652..78718466hg38UCSC Ensembl
Innerchr2:78841778..78945592hg19UCSC Ensembl
Innerchr2:78695286..78799100hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38103815
hg19103815
hg18103815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732005
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)nsv1002153
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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