A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621665



Internal ID7008533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121570762..121576516hg38UCSC Ensembl
Innerchr9:121570765..121576514hg38UCSC Ensembl
Outerchr9:121570760..121576519hg38UCSC Ensembl
chr9:124333041..124338795hg19UCSC Ensembl
Innerchr9:124333044..124338793hg19UCSC Ensembl
Outerchr9:124333039..124338798hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg385755
hg195755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13615531, essv13615526, essv13615523, essv13615533, essv13615529, essv13615524, essv13615527, essv13615530, essv13615525, essv13615528, essv13615535, essv13615534, essv13615532, essv13615522
SamplesHG03111, HG03298, NA20298, HG03168, HG02325, HG03169, NA19236, HG02450, HG02307, HG03301, HG03367, NA18865, HG02941, HG02970
Known GenesDAB2IP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621665
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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