A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1057783



Internal ID15564283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33749993..33811187hg38UCSC Ensembl
Innerchr6:33717770..33778964hg19UCSC Ensembl
Innerchr6:33825748..33886942hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3861195
hg1961195
hg1861195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv602839
Supporting Variants
Samples
Known GenesLEMD2, MLN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1057783
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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