A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033647



Internal ID19122868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111126694..111283380hg38UCSC Ensembl
Innerchr7:110766750..110923436hg19UCSC Ensembl
Innerchr7:110553986..110710672hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38156687
hg19156687
hg18156687
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645220
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)nsv1033647
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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