A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3751485



Internal ID19049766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110715730..110742009hg38UCSC Ensembl
Innerchr7:110355786..110382065hg19UCSC Ensembl
Innerchr7:110143022..110169301hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3826280
hg1926280
hg1826280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1017305
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3751485
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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