A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv600832



Internal ID16041555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:2945097..2970334hg38UCSC Ensembl
Innerchr6:2945331..2970568hg19UCSC Ensembl
Innerchr6:2890330..2915567hg18UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3825238
hg1925238
hg1825238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1048672
Samples
Known GenesSERPINB6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv600832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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