A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985927



Internal ID12984244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:17593302..17632502hg38UCSC Ensembl
Innerchr9:17593300..17632500hg19UCSC Ensembl
Innerchr9:17583300..17622500hg18UCSC Ensembl
Innerchr9:17583300..17622500hg17UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3839201
hg1939201
hg1839201
hg1739201
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752287
Supporting Variants
SamplesSPC_85
Known GenesSH3GL2
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985927
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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