A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695682



Internal ID15432334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155097176..155211883hg38UCSC Ensembl
InnerchrX:154325451..154440161hg19UCSC Ensembl
InnerchrX:153978645..154093355hg18UCSC Ensembl
InnerchrX:153889155..154003865hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38114708
hg19114711
hg18114711
hg17114711
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518251
Supporting Variants
Samples
Known GenesBRCC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695682
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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