A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009796



Internal ID18752327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195016604..195403519hg38UCSC Ensembl
Innerchr3:194737333..195124248hg19UCSC Ensembl
Innerchr3:196218622..196605537hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38386916
hg19386916
hg18386916
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3611379
Samples
Known GenesACAP2, XXYLT1, XXYLT1-AS1, XXYLT1-AS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009796
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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