A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv795955



Internal ID16089911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:51820741..51822032hg38UCSC Ensembl
Innerchr12:52214525..52215816hg19UCSC Ensembl
Innerchr12:50500792..50502083hg18UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg381292
hg191292
hg181292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv558889
Supporting Variants
Samples
Known GenesFIGNL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv795955
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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