A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5384256



Internal ID8475991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:97289149..97290706hg38UCSC Ensembl
Outerchr7:96918461..96920018hg19UCSC Ensembl
Outerchr7:96756397..96757954hg18UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg381558
hg191558
hg181558
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2560635
Supporting Variants
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)essv5384256
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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