A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999960



Internal ID19159496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:101609554..101643393hg38UCSC Ensembl
Innerchr2:102226016..102259855hg19UCSC Ensembl
Innerchr2:101592448..101626287hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg3833840
hg1933840
hg1833840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3580099
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999960
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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