A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787997



Internal ID18819712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89204468..90033564hg38UCSC Ensembl
Innerchr6:89914187..90743283hg19UCSC Ensembl
Innerchr6:89970906..90800004hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38829097
hg19829097
hg18829099
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 Human OmniExpress
CommentsNumber of probes=230
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787997
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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