A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066574



Internal ID19155793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43003881..43249346hg38UCSC Ensembl
Innerchr19:43508033..43753498hg19UCSC Ensembl
Innerchr19:48199873..48445338hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38245466
hg19245466
hg18245466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3583n100
Supporting Variantsnssv3571704, nssv3571698, nssv3571715, nssv3571710, nssv3571708, nssv3571699, nssv3571696, nssv3571717, nssv3571706, nssv3571709, nssv3571703, nssv3571697, nssv3571713, nssv3571716, nssv3571714, nssv3571701, nssv3571711, nssv3571702, nssv3571712, nssv3571700, nssv3571719, nssv3571718, nssv3571707, nssv3571705
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066574
Frequency
Sample Size11257
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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