A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702600



Internal ID15092566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152892328..152932224hg38UCSC Ensembl
InnerchrX:152060872..152100768hg19UCSC Ensembl
InnerchrX:151811528..151851424hg18UCSC Ensembl
InnerchrX:151731440..151771336hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3839897
hg1939897
hg1839897
hg1739897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517284
Supporting Variants
Samples
Known GenesZNF185
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702600
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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