A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584702



Internal ID16025425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:233335749..233379402hg38UCSC Ensembl
Innerchr2:234244395..234288048hg19UCSC Ensembl
Innerchr2:233909134..233952787hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3843654
hg1943654
hg1843654
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7339n54
Supporting Variantsnssv1150765
Samples1780862093_A
Known GenesDGKD, SAG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584702
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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