A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1075e199



Internal ID22758848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10657012..10660647hg38UCSC Ensembl
chr6:10657245..10660880hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg383636
hg193636
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2666334, esv2666483
SamplesHG00626, NA19701, HG00542, HG00442, HG00671, NA18508, NA18486, HG00566, NA18530, NA18616, HG00654, HG00693, NA19446, NA19373, HG00501, NA18923, NA19904, HG00512, HG00683, NA19372, NA19901, NA19451, NA19908, HG00629, NA18538, HG01171, HG00596, HG00428, NA19347, HG00653, HG00657, NA19236, NA18871, NA18534, HG00708, NA19000, HG00525, NA20282, HG00704, NA18523, NA19395, NA19436, HG00625, HG00607, HG00662, NA18615, NA19818, HG00656, HG00343, NA19900, NA18488, HG00628, NA19074, HG00437, HG00581, HG00593
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1075e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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