A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3544172



Internal ID18842453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41266750..41282098hg38UCSC Ensembl
Innerchr17:39423002..39438350hg19UCSC Ensembl
Innerchr17:36676528..36691876hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3815349
hg1915349
hg1815349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1067034
Supporting Variants
Samples
Known GenesKRTAP9-7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3544172
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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