A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025264



Internal ID19114482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131347777..131410549hg38UCSC Ensembl
Innerchr7:131032536..131095308hg19UCSC Ensembl
Innerchr7:130683076..130745848hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3862773
hg1962773
hg1862773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6619n100
Supporting Variantsnssv3662194, nssv3662193, nssv3662195
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)nsv1025264
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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