A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061604



Internal ID18804135
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 StatusM
Merged Variants
Supporting Variantsnssv3566525
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)nsv1061604
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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