A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604433



Internal ID16045156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104863741..104997489hg38UCSC Ensembl
Innerchr6:105311616..105445364hg19UCSC Ensembl
Innerchr6:105418309..105552057hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38133749
hg19133749
hg18133749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071877
Samples
Known GenesLIN28B, LINC00577
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604433
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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