A curated catalogue of human genomic structural variation




Variant Details

Variant: essv84214



Internal ID11650211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9337250..9365185hg38UCSC Ensembl
Innerchr17:9240567..9268502hg19UCSC Ensembl
Innerchr17:9181292..9209227hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3827936
hg1927936
hg1827936
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv29975
Supporting Variants
SamplesHuRef
Known GenesSTX8
MethodMerging
AnalysisNo Reference, merging experiment
PlatformNot Reported
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv84214
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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