A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023666



Internal ID19112883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61520009..61597238hg38UCSC Ensembl
Innerchr9:44727847..44805076hg19UCSC Ensembl
Innerchr9:44667843..44745072hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3877230
hg1977230
hg1877230
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7599n100
Supporting Variantsnssv3757604, nssv3691953, nssv3691955, nssv3691954
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)nsv1023666
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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