A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661061



Internal ID9927166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:30738388..30739272hg38UCSC Ensembl
chr8:30595905..30596789hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5940602, essv5868010, essv5944890, essv6488564, essv6334046, essv5755516, essv5571034, essv6151119, essv5441950, essv6355006, essv5458449, essv6268215, essv6387512, essv6447646, essv6151436, essv5822922, essv5730404, essv5626948, essv5441918, essv6175540, essv6310034, essv6037739, essv5586234, essv6500734, essv6022846, essv6492478, essv6443380, essv6313856, essv6184060
SamplesHG01462, HG00242, HG00315, HG00151, HG00244, HG00566, NA18530, NA12399, NA12413, HG00122, NA19723, HG01083, HG00335, NA20812, HG01133, HG00323, HG01353, HG00268, NA19462, HG00344, NA19081, NA19059, NA19009, HG00353, NA19439, HG00478, NA19065, NA18549, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661061
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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