A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025392



Internal ID18767924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:19381646..19478974hg38UCSC Ensembl
Innerchr9:19381644..19478972hg19UCSC Ensembl
Innerchr9:19371644..19468972hg18UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3897329
hg1997329
hg1897329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690684
Samples
Known GenesACER2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025392
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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