A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999970



Internal ID16946236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:37344798..37366197hg38UCSC Ensembl
Outerchr20:35973201..35994600hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3821400
hg1921400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954031
Supporting Variants
SamplesBILGI_BIOE
Known GenesSRC
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999970
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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