A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703487



Internal ID15093453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:100417088..100467096hg38UCSC Ensembl
Innerchr7:100014711..100064719hg19UCSC Ensembl
Innerchr7:99852647..99902655hg18UCSC Ensembl
Innerchr7:99659362..99709370hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3850009
hg1950009
hg1850009
hg1750009
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527107
Supporting Variants
Samples
Known GenesC7orf61, MEPCE, PPP1R35, TSC22D4, ZCWPW1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703487
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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