A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611037



Internal ID16398446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39403008..39492936hg38UCSC Ensembl
Innerchr8:39260527..39350455hg19UCSC Ensembl
Innerchr8:39379684..39469612hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3889929
hg1989929
hg1889929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12103n54
Supporting Variantsnssv1111158
Samples
Known GenesADAM3A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611037
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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