A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660866



Internal ID9926971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23643248..23645191hg38UCSC Ensembl
chr16:23654569..23656512hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5517123, essv6335546, essv6214592, essv6589919, essv5958970, essv6309625, essv6529495, essv5482976, essv5663058, essv6188248, essv5599598, essv6266787, essv6513987, essv5479454, essv5865656, essv6037752, essv6034689, essv5538143, essv6321650, essv6526275, essv5482082, essv5846131, essv6499493, essv5760009
SamplesHG00306, NA19057, HG00177, HG00272, NA18597, NA18558, HG00330, NA18611, NA18977, HG00325, HG00543, NA18544, NA18613, HG00657, NA18566, HG00324, HG00331, HG00613, NA18632, HG00672, HG00614, HG00421, HG00280, NA18624
Known GenesDCTN5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660866
Frequency
Sample Size1151
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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