A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997921



Internal ID19157457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34759898..34830233hg38UCSC Ensembl
Innerchr4:34761520..34831855hg19UCSC Ensembl
Innerchr4:34437915..34508250hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3870336
hg1970336
hg1870336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5165n100
Supporting Variantsnssv3620672, nssv3620673
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997921
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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