A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892998



Internal ID18837132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35106468..35295755hg38UCSC Ensembl
Outerchr17:35106468..35295755hg38UCSC Ensembl
Innerchr17:33433487..33622774hg19UCSC Ensembl
Outerchr17:33433487..33622774hg19UCSC Ensembl
Innerchr17:30457600..30646887hg18UCSC Ensembl
Outerchr17:30457600..30646887hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38189288
hg19189288
hg18189288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800819
Samples
Known GenesFNDC8, NLE1, RAD51D, RAD51L3-RFFL, SLC35G3, SLFN5, UNC45B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892998
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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