A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv557950



Internal ID15998673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:29691924..29693084hg38UCSC Ensembl
Innerchr12:29844857..29846017hg19UCSC Ensembl
Innerchr12:29736124..29737284hg18UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381161
hg191161
hg181161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2448n54
Supporting Variantsnssv790824, nssv790825
Samples
Known GenesTMTC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv557950
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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