A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021604



Internal ID19110822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132975997..133036084hg38UCSC Ensembl
Innerchr4:133897152..133957239hg19UCSC Ensembl
Innerchr4:134116602..134176689hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3860088
hg1960088
hg1860088
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5395n100
Supporting Variantsnssv3639528
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)nsv1021604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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