A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792024



Internal ID18827769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89206381..90025189hg38UCSC Ensembl
Innerchr6:89916100..90734908hg19UCSC Ensembl
Innerchr6:89972819..90791629hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38818809
hg19818809
hg18818811
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890901
Supporting Variants
Samples
Known GenesANKRD6, BACH2, CASP8AP2, GABRR1, GABRR2, GJA10, LYRM2, MDN1, RRAGD, UBE2J1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=261
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792024
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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