A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979254



Internal ID12633193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:67925146..68152450hg38UCSC Ensembl
Innerchr4:68790864..69018168hg19UCSC Ensembl
Innerchr4:68473459..68700763hg18UCSC Ensembl
Innerchr4:68619630..68846934hg17UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38227305
hg19227305
hg18227305
hg17227305
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35010
Supporting Variants
SamplesNA18517
Known GenesLOC550113, SYT14L, TMPRSS11A, TMPRSS11F, TMPRSS11GP
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979254
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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