A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032950



Internal ID19122172
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 StatusM
Merged Variants
Supporting Variantsnssv3654814, nssv3654813, nssv3654812
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)nsv1032950
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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