A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640084



Internal ID7026862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15773497..15791827hg38UCSC Ensembl
Innerchr17:15773497..15791827hg38UCSC Ensembl
Outerchr17:15772997..15792327hg38UCSC Ensembl
chr17:15676811..15695141hg19UCSC Ensembl
Innerchr17:15676811..15695141hg19UCSC Ensembl
Outerchr17:15676311..15695641hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3818331
hg1918331
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15625311, essv15625314, essv15625309, essv15625303, essv15625315, essv15625301, essv15625308, essv15625304, essv15625302, essv15625300, essv15625310, essv15625306, essv15625313, essv15625299, essv15625312, essv15625316, essv15625307, essv15625305
SamplesHG02337, HG03558, HG02895, HG03478, NA19131, HG03479, NA19917, HG02716, NA19236, HG01889, HG03476, NA19099, NA18865, HG03084, NA20289, HG03077, HG01883, HG03439
Known GenesMEIS3P1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640084
Frequency
Sample Size2504
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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