A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062704



Internal ID18805235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43159205..43342230hg38UCSC Ensembl
Innerchr19:43663357..43846382hg19UCSC Ensembl
Innerchr19:48355197..48538222hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38183026
hg19183026
hg18183026
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574249, nssv3724626, nssv3574250, nssv3574248, nssv3724628, nssv3724627
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062704
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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