A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672984



Internal ID15062950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88714632..88740797hg38UCSC Ensembl
Innerchr16:88781040..88807205hg19UCSC Ensembl
Innerchr16:87308541..87334706hg18UCSC Ensembl
Innerchr16:87308541..87334706hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3826166
hg1926166
hg1826166
hg1726166
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517643
Supporting Variants
Samples
Known GenesCTU2, LOC100289580, MIR4722, PIEZO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672984
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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