A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028722



Internal ID19117940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131369169..131417190hg38UCSC Ensembl
Innerchr7:131053928..131101949hg19UCSC Ensembl
Innerchr7:130704468..130752489hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3848022
hg1948022
hg1848022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6620n100
Supporting Variantsnssv3662198
Samples
Known GenesMKLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028722
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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