A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779298



Internal ID19182973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:126817725..126862973hg38UCSC Ensembl
Innerchr7:126457779..126503027hg19UCSC Ensembl
Innerchr7:126245015..126290263hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3845249
hg1945249
hg1845249
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891206
Supporting Variants
Samples
Known GenesGRM8
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779298
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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