A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027743



Internal ID19116961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:61554104..61647887hg38UCSC Ensembl
Innerchr9:44761942..44855725hg19UCSC Ensembl
Innerchr9:44701938..44795721hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3893784
hg1993784
hg1893784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7612n100
Supporting Variantsnssv3761508
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)nsv1027743
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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