A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004845



Internal ID19094062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44964987..45003835hg38UCSC Ensembl
Innerchr4:44967004..45005852hg19UCSC Ensembl
Innerchr4:44661761..44700609hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3838849
hg1938849
hg1838849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3625094, nssv3625095
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)nsv1004845
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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