A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604131



Internal ID16391540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91276024..91394960hg38UCSC Ensembl
Innerchr6:91985742..92104678hg19UCSC Ensembl
Innerchr6:92042463..92161399hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38118937
hg19118937
hg18118937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10838n54
Supporting Variantsnssv1068398
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604131
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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