A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779982



Internal ID19163043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111419830..111711456hg38UCSC Ensembl
Innerchr7:111059886..111351512hg19UCSC Ensembl
Innerchr7:110847122..111138748hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38291627
hg19291627
hg18291627
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891183
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=54
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779982
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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