A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567508



Internal ID18865789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41462891..41550966hg38UCSC Ensembl
Innerchr19:41968797..42057334hg19UCSC Ensembl
Innerchr19:46660637..46749174hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3888076
hg1988538
hg1888538
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055515
Supporting Variants
Samples
Known GenesLOC100505495
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567508
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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