A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033819



Internal ID19123040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39481989..39529434hg38UCSC Ensembl
Innerchr8:39339508..39386953hg19UCSC Ensembl
Innerchr8:39458665..39506110hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3847446
hg1947446
hg1847446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7182n100
Supporting Variantsnssv3687206
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033819
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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