A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749554



Internal ID19047835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141711567..141771158hg38UCSC Ensembl
Innerchr6:142032704..142092295hg19UCSC Ensembl
Innerchr6:142074397..142133988hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3859592
hg1959592
hg1859592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1019046
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)nssv3749554
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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