A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525441



Internal ID18477036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86808989..88365666hg38UCSC Ensembl
Innerchr13:87461244..89017921hg19UCSC Ensembl
Innerchr13:86259245..87815922hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg381556678
hg191556678
hg181556678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044071
Supporting Variants
Samples
Known GenesLINC00397, MIR4500, MIR4500HG, SLITRK5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525441
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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