A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566525



Internal ID18518120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28373028..29773397hg38UCSC Ensembl
Innerchr19:28863935..30264304hg19UCSC Ensembl
Innerchr19:33555775..34956144hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381400370
hg191400370
hg181400370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061604
Supporting Variants
Samples
Known GenesC19orf12, LINC00906, LOC100505835, LOC284395, PLEKHF1, POP4, UQCRFS1, VSTM2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566525
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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