A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608680



Internal ID6648913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35521204..35600518hg38UCSC Ensembl
chr6:35488981..35568295hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3879315
hg1979315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12315581, essv12315576, essv12315592, essv12315586, essv12315578, essv12315573, essv12315575, essv12315582, essv12315587, essv12315574, essv12315588, essv12315577, essv12315590, essv12315584, essv12315572, essv12315580, essv12315583, essv12315593, essv12315589, essv12315585, essv12315571, essv12315579, essv12315591
SamplesHG00114, HG02337, NA19107, HG03572, HG03135, HG02541, NA19197, HG02111, NA19172, HG02471, NA19200, HG02678, HG03428, HG01092, HG03202, HG02455, HG03117, HG01342, NA19818, HG01086, HG03112, HG03470, NA19316
Known GenesFKBP5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608680
Frequency
Sample Size2504
Observed Gain23
Observed Loss0
Observed Complex0
Frequencyn/a


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