A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557476



Internal ID18509071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46202822..46358076hg38UCSC Ensembl
Innerchr17:44280188..44435442hg19UCSC Ensembl
Innerchr17:41635965..41791184hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38155255
hg19155255
hg18155220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064242
Supporting Variants
Samples
Known GenesARL17A, ARL17B, KANSL1, LOC644172, LRRC37A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557476
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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