A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3632n54



Internal ID22771527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35534045..35535507hg38UCSC Ensembl
chr14:36003251..36004713hg19UCSC Ensembl
chr14:35073002..35074464hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381463
hg191463
hg181463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv564335, nsv564330
Samples
Known GenesINSM2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3632n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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