A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056092



Internal ID18798623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54786419..54852057hg38UCSC Ensembl
Innerchr19:55297871..55363512hg19UCSC Ensembl
Innerchr19:59989683..60055324hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3865639
hg1965642
hg1865642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3676n100
Supporting Variantsnssv3570342
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056092
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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