A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701127



Internal ID15091093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87905781..88183653hg38UCSC Ensembl
Innerchr7:87535096..87812968hg19UCSC Ensembl
Innerchr7:87373032..87650904hg18UCSC Ensembl
Innerchr7:87179747..87457619hg17UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38277873
hg19277873
hg18277873
hg17277873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525073
Supporting Variants
Samples
Known GenesADAM22, DBF4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701127
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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