A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022230



Internal ID19111448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39833345hg38UCSC Ensembl
Innerchr9:41600370..41978363hg19UCSC Ensembl
Innerchr9:41590370..41968363hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38377994
hg19377994
hg18377994
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7547n100
Supporting Variantsnssv3755949, nssv3690223, nssv3690222
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)nsv1022230
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer