A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654813



Internal ID18953094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:18830561..18859474hg38UCSC Ensembl
Innerchr6:18830792..18859705hg19UCSC Ensembl
Innerchr6:18938771..18967684hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3828914
hg1928914
hg1828914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032950
Supporting Variants
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)nssv3654813
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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