A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566596



Internal ID18864877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:34825081..34882835hg38UCSC Ensembl
Innerchr19:35315985..35373739hg19UCSC Ensembl
Innerchr19:40007825..40065579hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3857755
hg1957755
hg1857755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059180
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)nssv3566596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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