A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010714



Internal ID18753246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:77821351..78069876hg38UCSC Ensembl
Innerchr4:78742505..78991030hg19UCSC Ensembl
Innerchr4:78961529..79210054hg18UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38248526
hg19248526
hg18248526
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633878
Samples
Known GenesFRAS1, MRPL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010714
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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