A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150007



Internal ID15507988
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
Samples1780862275_A
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)nssv1150007
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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