A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043967



Internal ID19133186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:101736382..101874046hg38UCSC Ensembl
Innerchr9:104498664..104636328hg19UCSC Ensembl
Innerchr9:103538485..103676149hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38137665
hg19137665
hg18137665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697578
Samples
Known GenesGRIN3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043967
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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