A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047708



Internal ID19136927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:132824476..132853814hg38UCSC Ensembl
Innerchr9:135699863..135729201hg19UCSC Ensembl
Innerchr9:134689684..134719022hg18UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3829339
hg1929339
hg1829339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3696405
Samples
Known GenesAK8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047708
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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