A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604261



Internal ID16391670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100100743..100167776hg38UCSC Ensembl
Innerchr6:100548619..100615652hg19UCSC Ensembl
Innerchr6:100655340..100722373hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3867034
hg1967034
hg1867034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1070557
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604261
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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