A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564523



Internal ID18516118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46267660..46563264hg38UCSC Ensembl
Innerchr17:44345026..44640630hg19UCSC Ensembl
Innerchr17:41700803..41995946hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38295605
hg19295605
hg18295144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056925
Supporting Variants
Samples
Known GenesARL17A, ARL17B, LRRC37A, LRRC37A2, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564523
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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