A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699578



Internal ID15436230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140856435..140981130hg38UCSC Ensembl
InnerchrX:139938600..140063295hg19UCSC Ensembl
InnerchrX:139766266..139890961hg18UCSC Ensembl
InnerchrX:139664120..139788815hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38124696
hg19124696
hg18124696
hg17124696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523758
Supporting Variants
Samples
Known GenesMIR320D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699578
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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