A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025681



Internal ID19114899
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 StatusM
Merged Variants
Supporting Variantsnssv3745566
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)nsv1025681
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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