A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009153



Internal ID19098371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:235977295..236020065hg38UCSC Ensembl
Innerchr2:236885939..236928709hg19UCSC Ensembl
Innerchr2:236550678..236593448hg18UCSC Ensembl
Cytoband2q37.2
Allele length
AssemblyAllele length
hg3842771
hg1942771
hg1842771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3586952
Samples
Known GenesAGAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009153
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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