A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780867



Internal ID18829284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:70913675..71083639hg38UCSC Ensembl
Innerchr5:70209502..70379466hg19UCSC Ensembl
Innerchr5:70245258..70415222hg18UCSC Ensembl
Cytoband5q13.2
Allele length
AssemblyAllele length
hg38169965
hg19169965
hg18169965
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890646
Supporting Variants
Samples
Known GenesGTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859, NAIP, SERF1A, SERF1B, SMN1, SMN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=29
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780867
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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