A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028064



Internal ID19117282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118100110..118152934hg38UCSC Ensembl
Innerchr7:117740164..117792988hg19UCSC Ensembl
Innerchr7:117527400..117580224hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3852825
hg1952825
hg1852825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6595n100
Supporting Variantsnssv3662057
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028064
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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