A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786024



Internal ID18822139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143731945..143784885hg38UCSC Ensembl
Innerchr7:143429038..143481978hg19UCSC Ensembl
Innerchr7:143059971..143112911hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3852941
hg1952941
hg1852941
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891222
Supporting Variants
Samples
Known GenesCTAGE6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=21
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786024
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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