A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621056



Internal ID7007926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91025327..91027110hg38UCSC Ensembl
Innerchr9:91025328..91027110hg38UCSC Ensembl
Outerchr9:91025327..91027111hg38UCSC Ensembl
chr9:93787609..93789392hg19UCSC Ensembl
Innerchr9:93787610..93789392hg19UCSC Ensembl
Outerchr9:93787609..93789393hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg381784
hg191784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13555520, essv13555515, essv13555525, essv13555518, essv13555524, essv13555521, essv13555523, essv13555516, essv13555517, essv13555519, essv13555522, essv13555514
SamplesHG01806, NA18618, HG02130, NA18747, NA18572, NA18626, HG02391, NA18615, HG00409, NA18989, HG02351, NA19063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621056
Frequency
Sample Size2504
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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