A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567826



Internal ID18519421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78852355..78901892hg38UCSC Ensembl
Innerchr17:76848437..76897974hg19UCSC Ensembl
Innerchr17:74360032..74409569hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3849538
hg1949538
hg1849538
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066843
Supporting Variants
Samples
Known GenesLOC100653515, TIMP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567826
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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