A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703347



Internal ID15439999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7036492..7127766hg38UCSC Ensembl
Innerchr3:7078179..7169453hg19UCSC Ensembl
Innerchr3:7053179..7144453hg18UCSC Ensembl
Innerchr3:7053179..7144453hg17UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3891275
hg1991275
hg1891275
hg1791275
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526975
Supporting Variants
Samples
Known GenesGRM7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703347
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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