A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999977



Internal ID16946243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:41335261..41367460hg38UCSC Ensembl
Outerchr20:39963901..39996100hg19UCSC Ensembl
Cytoband20q12
Allele length
AssemblyAllele length
hg3832200
hg1932200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954039
Supporting Variants
SamplesBILGI_BIOE
Known GenesEMILIN3, LPIN3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999977
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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