A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018075



Internal ID19107292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:64476069..64524973hg38UCSC Ensembl
Innerchr6:65185962..65234866hg19UCSC Ensembl
Innerchr6:65242683..65291587hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3848905
hg1948905
hg1848905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657650
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)nsv1018075
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer