A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999674



Internal ID16945940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:8220705..8241804hg38UCSC Ensembl
Outerchr12:8373301..8394400hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3821100
hg1921100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952794
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM86FP, FAM90A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999674
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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