A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891235



Internal ID18838945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150619826..150793996hg38UCSC Ensembl
Outerchr7:150603647..150799580hg38UCSC Ensembl
Innerchr7:150316914..150491084hg19UCSC Ensembl
Outerchr7:150300735..150496668hg19UCSC Ensembl
Innerchr7:149947847..150122017hg18UCSC Ensembl
Outerchr7:149931668..150127601hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38195934
hg19195934
hg18195934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778872, essv25782547, essv25781477
Samples
Known GenesGIMAP1, GIMAP1-GIMAP5, GIMAP2, GIMAP5, GIMAP6, TMEM176B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891235
Frequency
Sample Size3017
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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