A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014119



Internal ID18756652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107387583..108286989hg38UCSC Ensembl
Innerchr1:107930205..108829611hg19UCSC Ensembl
Innerchr1:107731728..108631134hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38899407
hg19899407
hg18899407
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv248n100
Supporting Variantsnssv3497336
Samples
Known GenesMIR7852, NBPF4, NTNG1, 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)nsv1014119
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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