A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566594



Internal ID18864875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34825081..34854959hg38UCSC Ensembl
Innerchr19:35315985..35345863hg19UCSC Ensembl
Innerchr19:40007825..40037703hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3829879
hg1929879
hg1829879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058294
Supporting Variants
Samples
Known GenesLOC400685
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566594
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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