A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009747



Internal ID19098966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:44964987..45004306hg38UCSC Ensembl
Innerchr4:44967004..45006323hg19UCSC Ensembl
Innerchr4:44661761..44701080hg18UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3839320
hg1939320
hg1839320
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5199n100
Supporting Variantsnssv3739385, nssv3739387, nssv3625104, nssv3625108, nssv3739392, nssv3625110, nssv3625106, nssv3739390, nssv3625119, nssv3625115, nssv3739391, nssv3625109, nssv3739394, nssv3625114, nssv3739393, nssv3625113, nssv3625116, nssv3625111, nssv3739388, nssv3625118, nssv3739384, nssv3739389, nssv3625112, nssv3625105, nssv3625117, nssv3625107, nssv3739386
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)nsv1009747
Frequency
Sample Size11257
Observed Gain27
Observed Loss0
Observed Complex0
Frequencyn/a


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