A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604145



Internal ID16391554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:92343861..92370241hg38UCSC Ensembl
Innerchr6:93053579..93079959hg19UCSC Ensembl
Innerchr6:93110300..93136680hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3826381
hg1926381
hg1826381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154184
SamplesHGDP00019
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604145
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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