A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998289



Internal ID19157825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:29408360..29481362hg38UCSC Ensembl
Innerchr4:29409982..29482984hg19UCSC Ensembl
Innerchr4:29019080..29092082hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3873003
hg1973003
hg1873003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737771
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)nsv998289
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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