A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017557



Internal ID19106774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64790655..64987600hg38UCSC Ensembl
Innerchr6:65500548..65697493hg19UCSC Ensembl
Innerchr6:65557269..65754214hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38196946
hg19196946
hg18196946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5996n100
Supporting Variantsnssv3657652
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)nsv1017557
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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