A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032787



Internal ID19122009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:131347777..131422147hg38UCSC Ensembl
Innerchr7:131032536..131106906hg19UCSC Ensembl
Innerchr7:130683076..130757446hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3874371
hg1974371
hg1874371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6619n100
Supporting Variantsnssv3662196
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)nsv1032787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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