A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695559



Internal ID15432211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:140812861..140922555hg38UCSC Ensembl
Innerchr7:140512661..140622355hg19UCSC Ensembl
Innerchr7:140159130..140268824hg18UCSC Ensembl
Innerchr7:139965845..140075539hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38109695
hg19109695
hg18109695
hg17109695
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518139
Supporting Variants
Samples
Known GenesBRAF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695559
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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