A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018405



Internal ID19107622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:9901840..9926287hg38UCSC Ensembl
Innerchr5:9901952..9926399hg19UCSC Ensembl
Innerchr5:9954952..9979399hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3824448
hg1924448
hg1824448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5567n100
Supporting Variantsnssv3638147, nssv3638152, nssv3638162, nssv3748667, nssv3638156, nssv3638150, nssv3638153, nssv3638159, nssv3748669, nssv3638161, nssv3638160, nssv3638165, nssv3638158, nssv3638155, nssv3638149, nssv3748668, nssv3638148, nssv3638157, nssv3638151, nssv3638154, nssv3638163, nssv3638164
Samples
Known GenesLOC285692
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018405
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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