A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778872



Internal ID18829421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150603647..150793996hg38UCSC Ensembl
Innerchr7:150300735..150491084hg19UCSC Ensembl
Innerchr7:149931668..150122017hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38190350
hg19190350
hg18190350
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891235
Supporting Variants
Samples
Known GenesGIMAP1, GIMAP1-GIMAP5, GIMAP2, GIMAP5, GIMAP6, TMEM176B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=59
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778872
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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