A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037750



Internal ID18780281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105265411..105489452hg38UCSC Ensembl
Innerchr9:108027692..108251733hg19UCSC Ensembl
Innerchr9:107067513..107291554hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38224042
hg19224042
hg18224042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697640
Samples
Known GenesFSD1L, SLC44A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037750
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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