A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026605



Internal ID19115823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:171484847..171585385hg38UCSC Ensembl
Innerchr4:172405998..172506536hg19UCSC Ensembl
Innerchr4:172642573..172743111hg18UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38100539
hg19100539
hg18100539
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5475n100
Supporting Variantsnssv3635433
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026605
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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