A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066225



Internal ID19155444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41462891..41501959hg38UCSC Ensembl
Innerchr19:41968797..42007875hg19UCSC Ensembl
Innerchr19:46660637..46699715hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3839069
hg1939079
hg1839079
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3547n100
Supporting Variantsnssv3567507
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)nsv1066225
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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