A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604319



Internal ID16391728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:101859194..101907992hg38UCSC Ensembl
Innerchr6:102307069..102355867hg19UCSC Ensembl
Innerchr6:102413762..102462560hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3848799
hg1948799
hg1848799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10873n54
Supporting Variantsnssv1070794
Samples
Known GenesGRIK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604319
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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