A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016628



Internal ID19105845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139336446..139396715hg38UCSC Ensembl
Innerchr4:140257600..140317869hg19UCSC Ensembl
Innerchr4:140477050..140537319hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3860270
hg1960270
hg1860270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5409n100
Supporting Variantsnssv3641185
Samples
Known GenesNAA15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016628
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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