A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv686848



Internal ID15076814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151983193..151987997hg38UCSC Ensembl
Innerchr6:152304328..152309132hg19UCSC Ensembl
Innerchr6:152346021..152350825hg18UCSC Ensembl
Innerchr6:152396442..152401246hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg384805
hg194805
hg184805
hg174805
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517009
Supporting Variants
Samples
Known GenesESR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv686848
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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