A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015666



Internal ID18758200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89446386..89678417hg38UCSC Ensembl
Innerchr6:90156105..90388136hg19UCSC Ensembl
Innerchr6:90212824..90444857hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38232032
hg19232032
hg18232034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6089n100
Supporting Variantsnssv3648955
Samples
Known GenesANKRD6, LYRM2, MDN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015666
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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