A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067032



Internal ID19156251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43029962..43217388hg38UCSC Ensembl
Innerchr19:43534114..43721540hg19UCSC Ensembl
Innerchr19:48225954..48413380hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38187427
hg19187427
hg18187427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3583n100
Supporting Variantsnssv3571750
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer