A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038107



Internal ID19127326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113119308..113148996hg38UCSC Ensembl
Innerchr9:115881588..115911276hg19UCSC Ensembl
Innerchr9:114921409..114951097hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3829689
hg1929689
hg1829689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7705n100
Supporting Variantsnssv3759812
Samples
Known GenesFAM225A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038107
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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