A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790582



Internal ID19175536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:63853627..64511352hg38UCSC Ensembl
Innerchr7:63314005..63971730hg19UCSC Ensembl
Innerchr7:62951440..63609165hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38657726
hg19657726
hg18657726
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891132
Supporting Variants
Samples
Known GenesLINC01005, YWHAEP1, ZNF679, ZNF727, ZNF735, ZNF736
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=129
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790582
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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