A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801555



Internal ID19176897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:80519352..80526998hg38UCSC Ensembl
Innerchr7:80148668..80156314hg19UCSC Ensembl
Innerchr7:79986604..79994250hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg387647
hg197647
hg187647
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891150
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801555
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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