A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv790824



Internal ID15738094
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 StatusS
Merged Variantsnsv557950
Supporting Variants
Samples
Known GenesTMTC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv790824
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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