A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998675



Internal ID16944941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:1561235..1573734hg38UCSC Ensembl
Outerchr8:1509401..1521900hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3812500
hg1912500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950273
Supporting Variants
SamplesBILGI_BIOE
Known GenesDLGAP2, LOC100507435
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998675
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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