A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044461



Internal ID19133680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:93599766..93635056hg38UCSC Ensembl
Innerchr9:96362048..96397338hg19UCSC Ensembl
Innerchr9:95401869..95437159hg18UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3835291
hg1935291
hg1835291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7688n100
Supporting Variantsnssv3759786
Samples
Known GenesPHF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044461
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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