A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002946



Internal ID16949212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:63322398..63328301hg38UCSC Ensembl
Outerchr2:63549533..63555436hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg385904
hg195904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954155
Supporting Variants
SamplesBILGI_BIOE
Known GenesWDPCP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002946
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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