A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1074462



Internal ID15927648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151297100..151300476hg38UCSC Ensembl
Innerchr6:151618235..151621611hg19UCSC Ensembl
Innerchr6:151659928..151663304hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg383377
hg193377
hg183377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604888
Supporting Variants
Samples
Known GenesAKAP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1074462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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