A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066604



Internal ID19155823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41348899..41371345hg38UCSC Ensembl
Innerchr17:39505151..39527597hg19UCSC Ensembl
Innerchr17:36758677..36781123hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3822447
hg1922447
hg1822447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3171n100
Supporting Variantsnssv3544210
Samples
Known GenesKRT33A, KRT33B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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