A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018499



Internal ID18761032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4665656..4706366hg38UCSC Ensembl
Innerchr9:4665656..4706366hg19UCSC Ensembl
Innerchr9:4655656..4696366hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3840711
hg1940711
hg1840711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692394
Samples
Known GenesCDC37L1, SPATA6L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018499
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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