A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704128



Internal ID15440780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:109212182..109258472hg38UCSC Ensembl
Innerchr6:109533385..109579675hg19UCSC Ensembl
Innerchr6:109640078..109686368hg18UCSC Ensembl
Innerchr6:109640078..109686368hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3846291
hg1946291
hg1846291
hg1746291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527657
Supporting Variants
Samples
Known GenesLOC100996634
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704128
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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