A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661597



Internal ID9927702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:35306479..35307509hg38UCSC Ensembl
chr14:35775685..35776715hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5821049, essv5963731, essv6028604, essv5737342, essv6475940, essv5773027, essv5778268, essv6226692, essv6020174, essv5778865, essv6272668, essv6329005, essv5482124, essv5481710, essv5427980, essv6536744, essv5711533, essv5836529, essv5518495, essv6394171, essv6120928, essv5574047, essv6573688, essv6269266, essv6126243, essv6050522, essv5554706, essv6496351
SamplesNA19700, NA19704, NA20752, NA18486, NA19057, NA19068, NA18519, NA18982, NA18942, NA20540, NA18571, HG00158, HG00512, HG00236, NA11994, NA19235, NA18867, NA19908, NA19070, NA19236, HG00250, HG00155, NA19679, NA19102, NA11843, NA19900, NA18983, NA18984
Known GenesPSMA6
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661597
Frequency
Sample Size1151
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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