A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022221



Internal ID18764755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:24436486..24510873hg38UCSC Ensembl
Innerchr8:24293999..24368386hg19UCSC Ensembl
Innerchr8:24349944..24424276hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3874388
hg1974388
hg1874333
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7141n100
Supporting Variantsnssv3685378
Samples
Known GenesADAM7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022221
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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