A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704657



Internal ID15094623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149831357..149839298hg38UCSC Ensembl
Innerchr6:150152493..150160434hg19UCSC Ensembl
Innerchr6:150194186..150202127hg18UCSC Ensembl
Innerchr6:150244607..150252548hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg387942
hg197942
hg187942
hg177942
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517022
Supporting Variants
Samples
Known GenesLRP11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704657
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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