A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601168



Internal ID16041891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:25346106..25393078hg38UCSC Ensembl
Innerchr6:25346334..25393306hg19UCSC Ensembl
Innerchr6:25454313..25501285hg18UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3846973
hg1946973
hg1846973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051357
Samples
Known GenesLRRC16A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601168
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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