A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576184



Internal ID16016907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82013189..82032605hg38UCSC Ensembl
Innerchr17:79971065..79990481hg19UCSC Ensembl
Innerchr17:77564354..77583770hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3819417
hg1919417
hg1819417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5800n54
Supporting Variantsnssv877118
Samples
Known GenesASPSCR1, LRRC45, RAC3, STRA13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576184
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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