A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3696758



Internal ID18648353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2777886..3286320hg38UCSC Ensembl
Innerchr1:2694433..3202884hg19UCSC Ensembl
Innerchr1:2684293..3192744hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg38508435
hg19508452
hg18508452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010950
Supporting Variants
Samples
Known GenesACTRT2, LINC00982, MIR4251, PRDM16, TTC34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3696758
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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