A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030674



Internal ID19119893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:186931664..187527933hg38UCSC Ensembl
Innerchr4:187852818..188449087hg19UCSC Ensembl
Innerchr4:188089812..188686081hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38596270
hg19596270
hg18596270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3635642
Samples
Known GenesLOC339975
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030674
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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