A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995999



Internal ID15234859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41339595..41514244hg38UCSC Ensembl
Innerchr17:39495847..39670496hg19UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38174650
hg19174650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483014
Supporting Variants
Samples
Known GenesKRT13, KRT15, KRT31, KRT32, KRT33A, KRT33B, KRT34, KRT35, KRT36, KRT37, KRT38, LOC100505782
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995999
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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