A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604128



Internal ID16391537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90295657..90296753hg38UCSC Ensembl
Innerchr6:91005376..91006472hg19UCSC Ensembl
Innerchr6:91062097..91063193hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg381097
hg191097
hg181097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10837n54
Supporting Variantsnssv1068395
Samples
Known GenesBACH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604128
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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