A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672145



Internal ID15408797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143632535..143654020hg38UCSC Ensembl
Innerchr6:143953672..143975157hg19UCSC Ensembl
Innerchr6:143995365..144016850hg18UCSC Ensembl
Innerchr6:143995365..144016850hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3821486
hg1921486
hg1821486
hg1721486
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517253
Supporting Variants
Samples
Known GenesPHACTR2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672145
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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