A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001538



Internal ID19090755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:116027714..116072269hg38UCSC Ensembl
Innerchr3:115746561..115791116hg19UCSC Ensembl
Innerchr3:117229251..117273806hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3844556
hg1944556
hg1844556
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3735267
Samples
Known GenesLSAMP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1001538
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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