A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3635633



Internal ID18587228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186328740..186613274hg38UCSC Ensembl
Innerchr4:187249894..187534428hg19UCSC Ensembl
Innerchr4:187486888..187771422hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38284535
hg19284535
hg18284535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016739
Supporting Variants
Samples
Known GenesF11-AS1, FAT1, MTNR1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3635633
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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