A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700174



Internal ID15436826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56343288..56416880hg38UCSC Ensembl
InnerchrX:56369721..56443313hg19UCSC Ensembl
InnerchrX:56386446..56460038hg18UCSC Ensembl
InnerchrX:56252742..56326334hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3873593
hg1973593
hg1873593
hg1773593
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524276
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700174
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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