A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695251



Internal ID18646846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:128536013..128581755hg38UCSC Ensembl
Innerchr9:131298292..131344034hg19UCSC Ensembl
Innerchr9:130338113..130383855hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3845743
hg1945743
hg1845743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044853
Supporting Variants
Samples
Known GenesGLE1, SPTAN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695251
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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