A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997647



Internal ID18810497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:3751070..3825288hg38UCSC Ensembl
Innerchr4:3752797..3827015hg19UCSC Ensembl
Innerchr4:3722595..3796813hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg3874219
hg1974219
hg1874219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616124
Samples
Known GenesADRA2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997647
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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