A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528311



Internal ID15455604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:136965860..136996054hg38UCSC Ensembl
Innerchr7:136650607..136680801hg19UCSC Ensembl
Innerchr7:136301147..136331341hg18UCSC Ensembl
Innerchr7:136107862..136138056hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3830195
hg1930195
hg1830195
hg1730195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704889
Samples
Known GenesCHRM2, LOC349160
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528311
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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