A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000151



Internal ID16946417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:57497089..57536488hg38UCSC Ensembl
Outerchr16:57531001..57570400hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3839400
hg1939400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952683
Supporting Variants
SamplesBILGI_BIOE
Known GenesCCDC102A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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