A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv611007



Internal ID16398416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39380149..39492936hg38UCSC Ensembl
Innerchr8:39237668..39350455hg19UCSC Ensembl
Innerchr8:39356825..39469612hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38112788
hg19112788
hg18112788
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12102n54
Supporting Variantsnssv1110556, nssv1110559, nssv1110563, nssv1110555, nssv1110564, nssv1110557, nssv1110560, nssv1110558, nssv1110561, nssv1110562, nssv1110554
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv611007
Frequency
Sample Size17421
Observed Gain2
Observed Loss9
Observed Complex0
Frequencyn/a


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