A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015886



Internal ID18758420
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31480756..31512495hg38UCSC Ensembl
Innerchr6:31448533..31480272hg19UCSC Ensembl
Innerchr6:31556512..31588251hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3831740
hg1931740
hg1831740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655901
Samples
Known GenesMICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015886
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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