A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032974



Internal ID18775508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7106200..7353587hg38UCSC Ensembl
Innerchr7:7145831..7393218hg19UCSC Ensembl
Innerchr7:7112356..7359743hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38247388
hg19247388
hg18247388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752820
Samples
Known GenesC1GALT1, LOC101927354
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032974
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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