A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601164



Internal ID16041887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:24624863..24661371hg38UCSC Ensembl
Innerchr6:24625091..24661599hg19UCSC Ensembl
Innerchr6:24733070..24769578hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3836509
hg1936509
hg1836509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051355
Samples
Known GenesKIAA0319, TDP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601164
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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