A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023857



Internal ID19113074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61554104..61658190hg38UCSC Ensembl
Innerchr9:44761942..44866028hg19UCSC Ensembl
Innerchr9:44701938..44806024hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38104087
hg19104087
hg18104087
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7612n100
Supporting Variantsnssv3696825
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)nsv1023857
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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