A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007601



Internal ID19096820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:12269..51612hg38UCSC Ensembl
Innerchr4:12269..51506hg19UCSC Ensembl
Innerchr4:2269..41506hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3839344
hg1939238
hg1839238
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5053n100
Supporting Variantsnssv3619260, nssv3619255, nssv3619256, nssv3737923, nssv3619258, nssv3619257, nssv3619254, nssv3619259, nssv3619253, nssv3619261, nssv3737924
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)nsv1007601
Frequency
Sample Size11257
Observed Gain5
Observed Loss6
Observed Complex0
Frequencyn/a


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