A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064072



Internal ID18806603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54791531..54849083hg38UCSC Ensembl
Innerchr19:55302983..55360538hg19UCSC Ensembl
Innerchr19:59994795..60052350hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3857553
hg1957556
hg1857556
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3675n100
Supporting Variantsnssv3570412, nssv3570411
Samples
Known GenesKIR2DL4, KIR2DS4, KIR3DL1, LOC100287534
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064072
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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