A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030636



Internal ID19119855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65117744..65210761hg38UCSC Ensembl
Innerchr6:65827637..65920654hg19UCSC Ensembl
Innerchr6:65884358..65977375hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3893018
hg1993018
hg1893018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6000n100
Supporting Variantsnssv3657668
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)nsv1030636
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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