A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890950



Internal ID19185346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134194881..134233200hg38UCSC Ensembl
Outerchr6:134194881..134233200hg38UCSC Ensembl
Innerchr6:134516019..134554338hg19UCSC Ensembl
Outerchr6:134516019..134554338hg19UCSC Ensembl
Innerchr6:134557712..134596031hg18UCSC Ensembl
Outerchr6:134557712..134596031hg18UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3838320
hg1938320
hg1838320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787091
Samples
Known GenesSGK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890950
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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