A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021868



Internal ID19111086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131336032..131381658hg38UCSC Ensembl
Innerchr7:131020791..131066417hg19UCSC Ensembl
Innerchr7:130671331..130716957hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3845627
hg1945627
hg1845627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6618n100
Supporting Variantsnssv3662192
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)nsv1021868
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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