A curated catalogue of human genomic structural variation
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Variant Details
Variant: nsv1055505
Internal ID
18798036
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
Inner
chr17:46088437..46215377
hg38
UCSC
Ensembl
Inner
chr17:44165803..44292743
hg19
UCSC
Ensembl
Inner
chr17:41521621..41648520
hg18
UCSC
Ensembl
Cytoband
17q21.31
Allele length
Assembly
Allele length
hg38
126941
hg19
126941
hg18
126900
Variant Type
CNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
dgv3182n100
Supporting Variants
nssv3546376
,
nssv3546378
,
nssv3546379
,
nssv3546377
,
nssv3720318
,
nssv3546375
,
nssv3720319
,
nssv3546374
Samples
Known Genes
KANSL1
,
KANSL1-AS1
Method
SNP array
Analysis
Affymetrix SNP array copy number analysis
Platform
Affymetrix SNP Array 6.0
Comments
Reference
Coe_et_al_2014
Pubmed ID
25217958
Accession Number(s)
nsv1055505
Frequency
Sample Size
29084
Observed Gain
8
Observed Loss
0
Observed Complex
0
Frequency
n/a
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