A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007352



Internal ID19096571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227008801..227059459hg38UCSC Ensembl
Innerchr1:227196502..227247160hg19UCSC Ensembl
Innerchr1:225263125..225313783hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3850659
hg1950659
hg1850659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv580n100
Supporting Variantsnssv3492627
Samples
Known GenesCDC42BPA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007352
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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