A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005615



Internal ID19094832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:87273018..87303754hg38UCSC Ensembl
Innerchr4:88194170..88224906hg19UCSC Ensembl
Innerchr4:88413194..88443930hg18UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3830737
hg1930737
hg1830737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633926, nssv3633927, nssv3633928
Samples
Known GenesMIR5705
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1005615
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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