A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011093



Internal ID18753627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107774643..108219390hg38UCSC Ensembl
Innerchr1:108317265..108762012hg19UCSC Ensembl
Innerchr1:108118788..108563535hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38444748
hg19444748
hg18444748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3494321
Samples
Known GenesMIR7852, SLC25A24, VAV3, VAV3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011093
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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