A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017869



Internal ID19107086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:39455352..39878557hg38UCSC Ensembl
Innerchr9:41600370..42023575hg19UCSC Ensembl
Innerchr9:41590370..42013575hg18UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38423206
hg19423206
hg18423206
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7547n100
Supporting Variantsnssv3690227, nssv3690225, nssv3690226, nssv3690224
Samples
Known GenesKGFLP2, LOC643648, 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)nsv1017869
Frequency
Sample Size11257
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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