A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697462



Internal ID15434114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:2376042..2377643hg38UCSC Ensembl
Innerchr1:2307481..2309082hg19UCSC Ensembl
Innerchr1:2297341..2298942hg18UCSC Ensembl
Innerchr1:2339643..2341244hg17UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg381602
hg191602
hg181602
hg171602
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520511
Supporting Variants
Samples
Known GenesMORN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697462
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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