A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2623719



Internal ID8687277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:51334499..51336639hg38UCSC Ensembl
Outerchr6:51199297..51201437hg19UCSC Ensembl
Outerchr6:51307256..51309396hg18UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg382141
hg192141
hg182141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5195178
SamplesNA18507
Known Genes
MethodSequencing
AnalysisLarger insertions and deletions are found by looking at variation in mate pair distances in the 2x50 mate pair libraries. These data are included in separate files for each of three coverage values: 2.2x, 4.0x, 5.6x, and 8.4x
PlatformNot specified
CommentsoriginalFile=Yoruban_large_indels_8.4x.gff
ReferenceMcKernan_et_al_2009
Pubmed ID19546169
Accession Number(s)esv2623719
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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