A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696661



Internal ID15086627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:126110662..126117830hg38UCSC Ensembl
Innerchr3:125829505..125836673hg19UCSC Ensembl
Innerchr3:127312195..127319363hg18UCSC Ensembl
Innerchr3:127312203..127319371hg17UCSC Ensembl
Cytoband3q21.2
Allele length
AssemblyAllele length
hg387169
hg197169
hg187169
hg177169
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520037
Supporting Variants
Samples
Known GenesALDH1L1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696661
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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