A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv868918



Internal ID16162874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19384106..19387191hg38UCSC Ensembl
Innerchr17:19287419..19290504hg19UCSC Ensembl
Innerchr17:19228012..19231097hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383086
hg193086
hg183086
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574574
Supporting Variants
Samples
Known GenesMFAP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv868918
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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