A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033141



Internal ID19122363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39456483..39833345hg38UCSC Ensembl
Innerchr9:41601501..41978363hg19UCSC Ensembl
Innerchr9:41591501..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38376863
hg19376863
hg18376863
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7546n100
Supporting Variantsnssv3690237, nssv3690238
Samples
Known GenesKGFLP2, LOC653501, MGC21881
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033141
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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