A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021533



Internal ID19110751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111198556..111561468hg38UCSC Ensembl
Innerchr7:110838612..111201524hg19UCSC Ensembl
Innerchr7:110625848..110988760hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38362913
hg19362913
hg18362913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6566n100
Supporting Variantsnssv3645231
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)nsv1021533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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