A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670781



Internal ID15060747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35730150..35750059hg38UCSC Ensembl
Innerchr19:36221051..36240960hg19UCSC Ensembl
Innerchr19:40912891..40932800hg18UCSC Ensembl
Innerchr19:40912891..40932800hg17UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3819910
hg1919910
hg1819910
hg1719910
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515536
Supporting Variants
Samples
Known GenesIGFLR1, KMT2B, LIN37, PSENEN, U2AF1L4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670781
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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