A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149701



Internal ID15855787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36459737..36549567hg38UCSC Ensembl
Innerchr17:34815551..34905408hg19UCSC Ensembl
Innerchr17:31889664..31979521hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3889831
hg1989858
hg1889858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574909
Supporting Variants
Samples1782681378_A
Known GenesGGNBP2, MYO19, PIGW, ZNHIT3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149701
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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