A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696019



Internal ID15432671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:97474743..97513319hg38UCSC Ensembl
Innerchr5:96810447..96849023hg19UCSC Ensembl
Innerchr5:96836203..96874779hg18UCSC Ensembl
Innerchr5:96836203..96874779hg17UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3838577
hg1938577
hg1838577
hg1738577
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518575
Supporting Variants
Samples
Known GenesLOC102546227
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696019
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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