A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745566



Internal ID19043847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64930754..64990639hg38UCSC Ensembl
Innerchr6:65640647..65700532hg19UCSC Ensembl
Innerchr6:65697368..65757253hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3859886
hg1959886
hg1859886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025681
Supporting Variants
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3745566
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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