A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047528



Internal ID18790059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69071560..69102586hg38UCSC Ensembl
Innerchr9:71686476..71717502hg19UCSC Ensembl
Innerchr9:70876296..70907322hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3831027
hg1931027
hg1831027
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7667n100
Supporting Variantsnssv3696223
Samples
Known GenesFXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047528
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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