A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515485



Internal ID15443332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151709072..151709846hg38UCSC Ensembl
InnerchrX:150877544..150878318hg19UCSC Ensembl
InnerchrX:150628200..150628974hg18UCSC Ensembl
InnerchrX:150548112..150548886hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38775
hg19775
hg18775
hg17775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv654304, nssv687608, nssv669766, nssv674113, nssv665425, nssv667766, nssv686968, nssv693126, nssv672204, nssv672279, nssv677516, nssv681351, nssv665374, nssv653561, nssv687313, nssv668608, nssv651664, nssv678210
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515485
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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