A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521407



Internal ID15448700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150323206..150421502hg38UCSC Ensembl
Innerchr7:150020295..150118590hg19UCSC Ensembl
Innerchr7:149651228..149749523hg18UCSC Ensembl
Innerchr7:149457943..149556238hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3898297
hg1998296
hg1898296
hg1798296
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698017
Samples
Known GenesACTR3C, LOC728743, LRRC61, RARRES2, REPIN1, RNU6-33P, RNU6-34P, ZBED6CL, ZNF775
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521407
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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