A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057898



Internal ID18800429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54725768..54854163hg38UCSC Ensembl
Innerchr19:55237234..55365618hg19UCSC Ensembl
Innerchr19:59929046..60057430hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38128396
hg19128385
hg18128385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3668n100
Supporting Variantsnssv3574554
Samples
Known GenesKIR2DL1, KIR2DL3, KIR2DL4, KIR2DS4, KIR3DL1, KIR3DL2, KIR3DL3, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057898
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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