A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720860



Internal ID18672455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39706352..39753735hg38UCSC Ensembl
Innerchr17:37862605..37909988hg19UCSC Ensembl
Innerchr17:35116131..35163514hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3847384
hg1947384
hg1847384
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056234
Supporting Variants
Samples
Known GenesERBB2, GRB7, MIEN1, MIR4728
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3720860
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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