A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3648953



Internal ID18600548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:89093252..89253488hg38UCSC Ensembl
Innerchr6:89802971..89963207hg19UCSC Ensembl
Innerchr6:89859690..90019926hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38160237
hg19160237
hg18160237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023532
Supporting Variants
Samples
Known GenesGABRR1, PM20D2, SRSF12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3648953
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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