A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515718



Internal ID15443329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113898791..113997568hg38UCSC Ensembl
InnerchrX:113142068..113240802hg19UCSC Ensembl
InnerchrX:113028333..113127067hg18UCSC Ensembl
InnerchrX:112947822..113046556hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg3898778
hg1998735
hg1898735
hg1798735
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685432, nssv697544, nssv664543, nssv666620, nssv689387, nssv675788, nssv689109
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515718
Frequency
Sample Size2026
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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