A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025547



Internal ID19114765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:355524..381137hg38UCSC Ensembl
Innerchr6:355524..381137hg19UCSC Ensembl
Innerchr6:300524..326137hg18UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3825614
hg1925614
hg1825614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5907n100
Supporting Variantsnssv3654686, nssv3654687
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025547
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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