A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996277



Internal ID15581778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:176061851..176221440hg38UCSC Ensembl
Innerchr1:176030987..176190576hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38159590
hg19159590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv483037
Supporting Variants
Samples
Known GenesRFWD2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996277
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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