A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066866



Internal ID19156085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54756764..54828266hg38UCSC Ensembl
Innerchr19:55268216..55339721hg19UCSC Ensembl
Innerchr19:59960028..60031533hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3871503
hg1971506
hg1871506
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3671n100
Supporting Variantsnssv3574629, nssv3574621, nssv3574628, nssv3574624, nssv3574626, nssv3574630, nssv3574623, nssv3574627, nssv3574625, nssv3574622
Samples
Known GenesKIR2DL1, KIR2DL4, 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)nsv1066866
Frequency
Sample Size11257
Observed Gain4
Observed Loss6
Observed Complex0
Frequencyn/a


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