A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524262



Internal ID15451555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137303825..137305974hg38UCSC Ensembl
Innerchr7:136988572..136990721hg19UCSC Ensembl
Innerchr7:136639112..136641261hg18UCSC Ensembl
Innerchr7:136445827..136447976hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg382150
hg192150
hg182150
hg172150
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700159
Samples
Known GenesPTN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524262
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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