A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564176



Internal ID7035276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:101679031..101684939hg38UCSC Ensembl
Outerchr9:104441313..104447221hg19UCSC Ensembl
Outerchr9:103481134..103487042hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385909
hg195909
hg185909
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003325
Supporting Variants
SamplesHuRef
Known GenesGRIN3A
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564176
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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