A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150006



Internal ID15527804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81991355..82086850hg38UCSC Ensembl
Innerchr17:79949231..80044726hg19UCSC Ensembl
Innerchr17:77542520..77638015hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3895496
hg1995496
hg1895496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576183
Supporting Variants
SamplesHGDP00546
Known GenesASPSCR1, DCXR, DUS1L, FASN, GPS1, LRRC45, RAC3, RFNG, STRA13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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