A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv871848



Internal ID16165804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:42275938..42276764hg38UCSC Ensembl
Innerchr17:40427956..40428782hg19UCSC Ensembl
Innerchr17:37681482..37682308hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38827
hg19827
hg18827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575044
Supporting Variants
Samples
Known GenesSTAT5B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv871848
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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