A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1068391



Internal ID15574891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89552180..89685297hg38UCSC Ensembl
Innerchr6:90261899..90395016hg19UCSC Ensembl
Innerchr6:90318618..90451737hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38133118
hg19133118
hg18133120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604124
Supporting Variants
Samples
Known GenesANKRD6, LYRM2, MDN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1068391
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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