A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3749714



Internal ID19047995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:168787638..168818901hg38UCSC Ensembl
Innerchr6:169187733..169218996hg19UCSC Ensembl
Innerchr6:168929658..168960921hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3831264
hg1931264
hg1831264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033784
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)nssv3749714
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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