A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017419



Internal ID18759953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106536794..106549125hg38UCSC Ensembl
Innerchr6:106984669..106997000hg19UCSC Ensembl
Innerchr6:107091362..107103693hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3812332
hg1912332
hg1812332
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654279
Samples
Known GenesAIM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017419
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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