A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705301



Internal ID15095267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:162186196..162214113hg38UCSC Ensembl
Innerchr1:162155986..162183903hg19UCSC Ensembl
Innerchr1:160422610..160450527hg18UCSC Ensembl
Innerchr1:158887644..158915561hg17UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg3827918
hg1927918
hg1827918
hg1727918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516482
Supporting Variants
Samples
Known GenesNOS1AP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705301
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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