A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031627



Internal ID19120849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:5311555..5351468hg38UCSC Ensembl
Innerchr9:5311555..5351468hg19UCSC Ensembl
Innerchr9:5301555..5341468hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3839914
hg1939914
hg1839914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692416
Samples
Known GenesRLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031627
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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