A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527175



Internal ID15454468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135310364..135349626hg38UCSC Ensembl
Innerchr7:134995116..135034378hg19UCSC Ensembl
Innerchr7:134645656..134684918hg18UCSC Ensembl
Innerchr7:134452371..134491633hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3839263
hg1939263
hg1839263
hg1739263
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703570
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527175
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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