A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3695242



Internal ID18993523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126181994..126220371hg38UCSC Ensembl
Innerchr9:128944273..128982650hg19UCSC Ensembl
Innerchr9:127984094..128022471hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3838378
hg1938378
hg1838378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039035
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3695242
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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