A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030690



Internal ID19119909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140493059..140507200hg38UCSC Ensembl
Innerchr7:140192859..140207000hg19UCSC Ensembl
Innerchr7:139839328..139853469hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3814142
hg1914142
hg1814142
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664254, nssv3664252, nssv3664251, nssv3664253
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)nsv1030690
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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