A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019174



Internal ID18761708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:29163105..29499710hg38UCSC Ensembl
Innerchr7:29202721..29539326hg19UCSC Ensembl
Innerchr7:29169246..29505851hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38336606
hg19336606
hg18336606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643329
Samples
Known GenesCHN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019174
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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