A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671002



Internal ID15407654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:74901252..74906086hg38UCSC Ensembl
Innerchr18:72613208..72618042hg19UCSC Ensembl
Innerchr18:70742196..70747030hg18UCSC Ensembl
Innerchr18:70742196..70747030hg17UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg384835
hg194835
hg184835
hg174835
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516801
Supporting Variants
Samples
Known GenesZNF407
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671002
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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