A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893225



Internal ID15840495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7033954..7055083hg38UCSC Ensembl
Innerchr19:7033965..7055094hg19UCSC Ensembl
Innerchr19:6984965..7006094hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3821130
hg1921130
hg1821130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578492
Supporting Variants
Samples
Known GenesMBD3L2, MBD3L4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893225
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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