A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030072



Internal ID19119291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:50835015..50864744hg38UCSC Ensembl
Innerchr6:50802728..50832457hg19UCSC Ensembl
Innerchr6:50910687..50940416hg18UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg3829730
hg1929730
hg1829730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657454
Samples
Known GenesTFAP2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030072
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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