A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557477



Internal ID18509072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46202822..46383054hg38UCSC Ensembl
Innerchr17:44280188..44460420hg19UCSC Ensembl
Innerchr17:41635965..41815840hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38180233
hg19180233
hg18179876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067461
Supporting Variants
Samples
Known GenesARL17A, ARL17B, KANSL1, LOC644172, LRRC37A, NSFP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557477
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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