A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695372



Internal ID15432024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:91163093..91191646hg38UCSC Ensembl
Innerchr7:90792408..90820961hg19UCSC Ensembl
Innerchr7:90630344..90658897hg18UCSC Ensembl
Innerchr7:90437059..90465612hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3828554
hg1928554
hg1828554
hg1728554
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517959
Supporting Variants
Samples
Known GenesCDK14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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