A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055515



Internal ID19144734
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 StatusM
Merged Variants
Supporting Variantsnssv3567508
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)nsv1055515
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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