A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702174



Internal ID15438826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28904210..29134090hg38UCSC Ensembl
InnerchrX:28922327..29152207hg19UCSC Ensembl
InnerchrX:28832248..29062128hg18UCSC Ensembl
InnerchrX:28681984..28911864hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38229881
hg19229881
hg18229881
hg17229881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516364
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702174
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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