A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604180



Internal ID16391589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94517995..94665602hg38UCSC Ensembl
Innerchr6:95227713..95375320hg19UCSC Ensembl
Innerchr6:95284434..95432041hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38147608
hg19147608
hg18147608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154848
SamplesNINDS_147
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604180
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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