A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570688



Internal ID18868969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24201148..24338821hg38UCSC Ensembl
Innerchr19:24383950..24521623hg19UCSC Ensembl
Innerchr19:24175790..24313463hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38137674
hg19137674
hg18137674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057596
Supporting Variants
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)nssv3570688
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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