A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664661



Internal ID15401313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74706683..74725717hg38UCSC Ensembl
Innerchr7:74121014..74140051hg19UCSC Ensembl
Innerchr7:73758950..73777987hg18UCSC Ensembl
Innerchr7:73565665..73584702hg17UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3819035
hg1919038
hg1819038
hg1719038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517573
Supporting Variants
Samples
Known GenesGTF2I
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664661
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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