A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001481



Internal ID19090698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208738149..208777312hg38UCSC Ensembl
Innerchr2:209602873..209642036hg19UCSC Ensembl
Innerchr2:209311118..209350281hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3839164
hg1939164
hg1839164
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4161n100
Supporting Variantsnssv3585602
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)nsv1001481
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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