A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019397



Internal ID19108615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72430645..72660163hg38UCSC Ensembl
Innerchr7:71895630..72125148hg19UCSC Ensembl
Innerchr7:71533566..71763084hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38229519
hg19229519
hg18229519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3755313
Samples
Known GenesTYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019397
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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